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VRLA battery
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A valve regulated lead‐acid (VRLA) battery, commonly known as a sealed lead-acid (SLA) battery,[1] is a type of lead-acid battery characterized by a limited amount of electrolyte ("starved" electrolyte) absorbed in a plate separator or formed into a gel, proportioning of the negative and positive plates so that oxygen recombination is facilitated within the cell, and the presence of a relief valve that retains the battery contents independent of the position of the cells.[2]
There are two primary types of VRLA batteries: absorbent glass mat (AGM) and gel cell (gel battery).[3] Gel cells add silica dust to the electrolyte, forming a thick putty-like gel; AGM (absorbent glass mat) batteries feature fiberglass mesh between the battery plates, which serves to contain the electrolyte and separate the plates. Both types of VRLA batteries offer advantages and disadvantages compared to flooded vented lead-acid (VLA) batteries or each other.[4]
Due to their construction, the gel cell and AGM types of VRLA can be mounted in any orientation and do not require constant maintenance. The term "maintenance-free" is a misnomer, as VRLA batteries still require cleaning and regular functional testing. They are widely used in large portable electrical devices, off-grid power systems (including uninterruptible power systems), motor vehicles (as traction batteries for light electric vehicles such as golf carts and as starter or auxiliary batteries for heavier vehicles) and similar roles, where large amounts of storage are needed at a lower cost than other low-maintenance technologies like lithium ion.
History
[edit]The first lead-acid gel battery was invented by Elektrotechnische Fabrik Sonneberg in 1934.[5] The modern gel, or VRLA, battery was invented by Otto Jache of Sonnenschein in 1957.[6][7]
The first AGM cell was the Cyclon, patented by Gates Rubber Corporation in 1972 and now produced by EnerSys.[8]
The Cyclon was a spiral-wound cell with thin lead foil electrodes. A number of manufacturers adopted the technology to implement it in cells with conventional flat plates. In the mid-1980s, two UK companies, Chloride Group and Tungstone Products, simultaneously introduced "ten-year life" AGM batteries in capacities up to 400 Ah, stimulated by a British Telecom specification for backup batteries to support new digital exchanges.
In the same period, Gates acquired another UK company, Varley, specializing in aircraft and military batteries. Varley adapted the Cyclon lead foil technology to produce flat-plate batteries with exceptional high rate output. These gained approval for a variety of aircraft, including the BAE 125 and 146 business jets, the Harrier jump jet and its derivative the AV-8B, and some F16 variants, as the first alternatives to then standard nickel–cadmium (Ni-Cd) batteries.[6]
Basic principle
[edit]
Lead-acid cells consist of two plates of lead, which serve as electrodes, suspended in an electrolyte consisting of diluted sulfuric acid. VRLA cells have the same chemistry except that the electrolyte is immobilized. In AGMs, this is accomplished with a fiberglass mat; in gel batteries or "gel cells", the electrolyte is in the form of a paste-like gel created by adding silica and other gelling agents to the electrolyte.[9]
When a cell discharges, the lead and diluted acid undergo a chemical reaction that produces lead sulfate and water. When a cell is subsequently charged, the lead sulfate and water are turned back into lead and acid. In all lead-acid battery designs, charging current must be adjusted to match the ability of the battery to absorb the energy. If the charging current is too great, electrolysis will occur, decomposing water into hydrogen and oxygen, in addition to the intended conversion of lead sulfate and water into lead dioxide, lead, and sulfuric acid (the reverse of the discharge process). If these gases are allowed to escape, as in a conventional flooded cell, the battery will need to have water (or electrolyte) added from time to time. In contrast, VRLA batteries retain generated gases within the battery as long as the pressure remains within safe levels. Under normal operating conditions, the gases can then recombine within the battery itself, sometimes with the help of a catalyst, and no additional electrolyte is needed.[10][11] However, if the pressure exceeds safety limits, safety valves open to allow the excess gases to escape, and in doing so regulate the pressure back to safe levels (hence "valve regulated" in "VRLA").[12]
Construction
[edit]Each cell in a VRLA battery has a pressure relief valve that will activate when the battery starts building pressure of hydrogen gas, generally a result of being recharged.[12]
The cell covers typically have gas diffusers built into them, which allow safe dispersal of any excess hydrogen that may be formed during overcharge. They are not permanently sealed but are designated to be maintenance-free. They can be oriented in any manner, unlike normal lead-acid batteries, which must be kept upright to avoid acid spills and to keep the plates' orientation vertical. Cells may be operated with the plates horizontal (pancake style), which may improve cycle life.[13]
Absorbent glass mat (AGM)
[edit]AGM batteries differ from flooded lead-acid batteries in that the electrolyte is held in the glass mats, as opposed to freely flooding the plates. Very thin glass fibers are woven into a mat to increase the surface area enough to hold a sufficient amount of electrolyte on the cells for their lifetime. The fibers that compose the fine glass mat do not absorb and are not affected by the acidic electrolyte. These mats are wrung out 2–5% after being soaked in acids just prior to finish manufacturing.
The plates in an AGM battery may be of any shape. Some are flat, whereas others are bent or rolled. Both deep-cycle and starting type of AGM batteries are built into a rectangular case according to Battery Council International (BCI) battery code specifications.
AGM batteries are more resistant to self-discharging than conventional batteries within a wide range of temperatures.[14]
As with lead-acid batteries, in order to maximize the life of an AGM battery, it is important to follow the manufacturer's charging specifications. The use of a voltage-regulated charger is recommended.[15] There is a direct correlation between the depth of discharge (DOD) and the cycle life of the battery,[16] with differences between 500 and 1300 cycles, depending on DOD.
Gel battery
[edit]This section needs additional citations for verification. (December 2019) |

Originally a kind of gel battery was produced in the early 1930s for portable valve (tube) radio LT supply (2, 4, or 6 V) by adding silica to the sulfuric acid.[17] By this time, the glass case was being replaced by celluloid, and later, in the 1930s, other plastics. Earlier "wet" cells in glass jars used special valves to allow tilt from vertical to one horizontal direction, in 1927 to 1931 or 1932.[18] The gel cells were less likely to leak when the portable set was handled roughly.
A modern gel battery is a VRLA battery with a gelated electrolyte; the sulfuric acid is mixed with fumed silica, which makes the resulting mass gel-like and immobile. Unlike a flooded wet cell lead-acid battery, these batteries do not need to be kept upright. Gel batteries reduce the electrolyte evaporation, spillage (and subsequent corrosion problems) common to the wet cell battery, and boast greater resistance to shock and vibration. Chemically, they are almost the same as wet (non-sealed) batteries except that the antimony in the lead plates is replaced by calcium, and gas recombination can take place.
Comparison: AGM vs. Gel
[edit]While both Absorbent Glass Mat (AGM) and Gel batteries are categorized as Valve-Regulated Lead-Acid (VRLA) batteries and are commonly used in vehicles and backup power systems, they differ in several key performance aspects. The comparison below highlights major differences based on characteristics such as charge speed, vibration resistance, and deep cycle capability.[19]
| Feature | AGM Battery | Gel Battery |
|---|---|---|
| Charging Speed | Fast | Slow |
| Discharge Rate | High | Low |
| Durability in Vibration | Excellent | Good |
| Performance in Extreme Heat | Good | Excellent |
| Deep Cycle Lifespan | Moderate | Long |
| Cost | Lower | Higher |
Applications
[edit]Many modern motorcycles and all-terrain vehicles (ATVs) on the market use AGM batteries to reduce the likelihood of acid spilling during cornering, vibration, or after accidents, and for packaging reasons. The lighter, smaller battery can be installed at an odd angle if needed for the design of the motorcycle. Due to the higher manufacturing costs compared with flooded lead-acid batteries, AGM batteries are currently used on luxury vehicles. As vehicles become heavier and equipped with more electronic devices such as navigation and stability control, AGM batteries are being employed to lower vehicle weight and provide better electrical reliability compared with flooded lead-acid batteries.
5 series BMWs from March 2007 incorporate AGM batteries in conjunction with devices for recovering brake energy using regenerative braking and computer control to ensure that the alternator charges the battery when the car is decelerating. Vehicles used in auto racing may use AGM batteries due to their vibration resistance. AGM batteries are also commonly used in classic vehicles, since they are much less likely to leak electrolyte, which could damage hard-to-replace body panels.
Deep-cycle AGMs are also commonly used in off-grid solar power and wind power installations as an energy storage bank and in large-scale amateur robotics, such as the FIRST and IGVC competitions.
AGM batteries are routinely chosen for remote sensors such as ice monitoring stations in the Arctic. AGM batteries, due to their lack of free electrolyte, will not crack and leak in these cold environments.
VRLA batteries are used extensively in power wheelchairs and mobility scooters, as the extremely low gas and acid output makes them much safer for indoor use. VRLA batteries are also used in uninterruptible power supplies (UPSs) as a backup when the electrical power goes off.
VRLA batteries are also the standard power source in sailplanes, due to their ability to withstand a variety of flight attitudes and a relatively large ambient temperature range with no adverse effects. However, charging regimes must be adapted with varying temperatures.[20]
VRLA batteries are used in the US Nuclear Submarine fleet, due to their power density, elimination of gassing, reduced maintenance, and enhanced safety.[21]
AGM and gel-cell batteries are also used for recreational marine purposes, with AGM being more commonly available. AGM deep-cycle marine batteries are offered by a number of suppliers. They typically are favored for their low-maintenance and spillproof qualities, although they are generally considered a less cost-effective solution relative to traditional flooded cells.
In telecommunications applications, VRLA batteries that comply with criteria in Telcordia Technologies requirements document GR-4228, Valve-Regulated Lead-Acid (VRLA) Battery String Certification Levels Based on Requirements for Safety and Performance, are recommended for deployment in the Outside Plant (OSP) at locations such as Controlled Environmental Vaults (CEVs), Electronic Equipment Enclosures (EEEs), and huts, and in uncontrolled structures such as cabinets. Relative to VRLA in telecommunications, the use of VRLA Ohmic Measurement Type Equipment (OMTE) and OMTE-like measurement equipment is a fairly new process to evaluate telecommunications battery plants.[22] The proper use of ohmic test equipment allows battery testing without the need to remove batteries from service to perform costly and time-consuming discharge tests.
Comparison with flooded lead-acid cells
[edit]VRLA gel and AGM batteries offer several advantages compared with VRLA flooded lead-acid and conventional lead-acid batteries. The battery can be mounted in any position, since the valves only operate on over-pressure faults. Since the battery system is designed to be recombinant and eliminate the emission of gases on overcharge, room ventilation requirements are reduced, and no acid fumes are emitted during normal operation. Flooded-cell gas emissions are of little consequence in all but the smallest confined areas and pose very little threat to a domestic user, so a wet-cell battery designed for longevity gives lower costs per kWh. In a gel battery, the volume of free electrolyte that could be released on damage to the case or venting is very small. There is no need (or ability) to check the level of electrolyte or to top up water lost due to electrolysis, thus reducing inspection and maintenance requirements.[23] Wet-cell batteries can be maintained by a self-watering system or by topping up every three months. The requirement to add distilled water is normally caused by overcharging. A well-regulated system should not require top-up more often than every three months.
All lead-acid batteries — charging requirements
[edit]An underlying disadvantage with all lead-acid (LA) batteries is the requirement for a relatively long recharge cycle time arising from an inherent three-stage charging process: bulk charge, absorption charge, and (maintenance) float charge stages. All lead-acid batteries, irrespective of type, are quick to bulk charge to about 70% of capacity, during which the battery will accept a large current input, determined at a voltage setpoint, within a few hours (with a charge source capable of supplying the design C-rate bulk stage current for a given Ah battery).
However, they then require a longer time spent in the current-tapering-off intermediate absorption charge stage after the initial bulk charge, when the LA battery charge acceptance rate gradually reduces and the battery will not accept a higher C-rate. When the absorption stage voltage setpoint is reached (and charge current has tapered off), the charger switches to a float voltage setpoint at a very low C-rate to maintain the battery's fully charged state indefinitely (the float stage offsets the battery's normal self-discharge over time).
If the charger fails to supply a sufficient absorption stage charge duration and C-rate (it 'plateaus' or times out, a common fault of cheap solar chargers) and a suitable float charge profile, the battery's capacity and longevity will be dramatically reduced.
To ensure maximum life, a lead-acid battery should be fully recharged as soon after a discharge cycle as possible to prevent sulfation, and kept at a full charge level by a float source when stored or idle (or stored dry new from the factory, an uncommon practice today).
When working a discharge cycle, a lead-acid battery should be kept at a depth-of-discharge (DOD) of less than 50%, ideally no more than 20–40% DOD; a true[24] LA deep-cycle battery can be taken to a lower DOD (even an occasional 80%), but these greater DOD cycles always impose a longevity price.
Lead-acid battery lifetime cycles will vary with the care given, and with the best care, they may achieve 500 to 1000 cycles. With less careful use, a lifetime as few as 100 cycles might be expected (all dependent upon the use environment too).
Charging sealed batteries
[edit]Because of calcium added to its plates to reduce water loss, a sealed AGM or gel battery recharges more quickly than a flooded lead-acid battery of either VRLA or conventional design.[25][26] Compared to flooded batteries, VRLA batteries are more vulnerable to thermal runaway during abusive charging. The electrolyte cannot be tested by hydrometer to diagnose improper charging that can reduce battery life.[26]
Comparison summary
[edit]AGM automobile batteries are typically about twice the price of flooded-cell batteries in a given BCI size group; gel batteries as much as five times the price.
AGM and gel VRLA batteries:
- Have a shorter recharge time than flooded lead-acid batteries;[27]
- Cannot tolerate overcharging (overcharging leads to premature failure);[27]
- Have a shorter useful life compared to properly maintained wet-cell batteries;[27]
- Discharge significantly less hydrogen gas;[27]
- Are by nature safer for the environment and safer to use;
- Can be used or positioned in any orientation.
See also
[edit]- List of battery types
- Sand battery
- Peukert's law – Law of capacity in lead-acid batteries
References
[edit]- ^ Eismin, Thomas K. (2013). Aircraft Electricity and Electronics (Sixth ed.). McGraw Hill Professional. p. 48. ISBN 978-0071799157.
- ^ Linden, David B.; Reddy, Thomas (2002). "24". Handbook of Batteries Third Edition. McGraw-Hill. ISBN 0-07-135978-8.
- ^ "Exploding Lead Acid Batteries, Mines Safety Bulletin No. 150". Australia: Queensland Government. 2015-10-27. Archived from the original on 2020-02-17. Retrieved 2020-02-17.
- ^ "Selecting the Proper Lead–Acid Technology" (PDF). Trojan Battery Company, California, USA. 2018. Archived (PDF) from the original on 2023-09-29. Retrieved 2023-09-29.
- ^ "A Brief History of Batteries and Stored Energy" (PDF). Netaworld.org. Archived from the original (PDF) on 20 February 2019. Retrieved 19 February 2019.
- ^ a b Desmond, Kevin (2016). "Jache, Otto". Innovators in Battery Technology: Profiles of 95 Influential Electrochemists. McFarland. ISBN 978-1476622781.
- ^ "Handbook for Gel-VRLA-Batteries : Part 1 : Basic Principles, Design, Features" (PDF). Sonnenschein.org. Retrieved 19 February 2019.
- ^ John Devitt (1997). "An account of the development of the first valve-regulated lead/acid cell". Journal of Power Sources. 64 (1–2): 153–156. Bibcode:1997JPS....64..153D. doi:10.1016/S0378-7753(96)02516-5.
- ^ Wagner, R (2004-03-09). "13.3 Gel batteries". In Moseley, Patrick T; et al. (eds.). Valve-Regulated Lead–Acid Batteries. Elsevier Science. p. 446. ISBN 9780444507464.
- ^ Robert Nelson, "The Basic Chemistry of Gas Recombination in Lead–Acid Batteries", JOM 53 (1) (2001)
- ^ "The Basic Chemistry of Gas Recombination in Lead–Acid Batteries". TMS.org.
- ^ a b Ronald Dell, David Anthony James Rand, Robert Bailey, Jr., Understanding Batteries, Royal Society of Chemistry, 2001, ISBN 0854046054 p. 101, pp.120-122
- ^ Vaccaro, F.J.; Rhoades, J.; Le, B.; Malley, R. (October 1998). "VRLA battery capacity cycling: Influences of physical design, materials, and methods to evaluate their effect". INTELEC - Twentieth International Telecommunications Energy Conference (Cat. No.98CH36263). pp. 166–172. doi:10.1109/INTLEC.1998.793494. ISBN 0-7803-5069-3. S2CID 108814630.
- ^ "Technical Manual: Powersports Batteries" (PDF). YuasaBatteries.com. GS Yuasa. Archived from the original (PDF) on 2017-07-12. Retrieved 2019-12-25.
- ^ "AGM Charging : Technical Support Desk". Support.rollsbattery.com. Retrieved 19 February 2019.
- ^ "AGM Discharge Characteristics : Modified on: Mon, 6 Oct, 2014". Support.rollsbattery.com. Retrieved 19 February 2019.
- ^ Watterson, Michael (2014-06-28). "Exide Gel-Cel Accumulator JSK2 Power-S Chloride Electrical". RadioMuseum.org. Retrieved 2015-03-01.
- ^ Walchhofer, Hans Martin; Watterson, Michael (2013-11-27). "Super Range Portable four A (without tuning dial)". RadioMuseum.org. Retrieved 2021-04-07.
- ^ "AGM vs Gel Battery – The Only Comparison You'll Ever Need". Powsea Battery. 2025-03-10. Retrieved 2025-04-10.
- ^ Linden, Reddy (ed), Handbook of batteries, third ed, 2002
- ^ "Exide Earns First-Ever Production Contract Awarded by U.S. Navy for Valve-Regulated Submarine Batteries; Shift to Advanced Product Prompts Closure of Kankakee, Illinois, Battery Plant". Business Wire. 2005. Retrieved 7 September 2016.
- ^ GR-3169-CORE, Generic Requirements for Valve-Regulated Lead–Acid (VRLA) Battery Ohmic Measurement Type Equipment (OMTE).
- ^ Fink, Donald G.; Beaty, H. Wayne (1978). Standard Handbook for Electrical Engineers (Eleventh ed.). New York: McGraw-Hill. pp. 11–116. ISBN 0-07-020974-X.
- ^ Collins, Rod (April 7, 2015). "What is a Deep Cycle Battery?".
- ^ Barre, Harold (1997). Managing 12 Volts: How to Upgrade, Operate and Troubleshoot 12 Volt Electrical Systems. Summer Breeze Publishing. p. 44. ISBN 978-0-9647386-1-4.(stating sealed battery plates are hardened with calcium to reduce water loss which "raises the batteries' internal resistance and prevents rapid charging.")
- ^ a b Sterling, Charles (2009). "FAQ: What is the Best Battery System to Use for an Auxiliary Charging System". Archived from the original on 16 March 2012. Retrieved 2 February 2012.
- ^ a b c d Calder, Nigel (1996). Boatowner's Mechanical and Electrical Manual (2nd ed.). International Marine. p. 11. ISBN 978-0-07-009618-9.
Further reading
[edit]Books and papers
[edit]- Valve-Regulated Lead–Acid Batteries. Edited by Patrick T. Moseley, Jurgen Garche, C.D. Parker, D.A.J. Rand. p202
- Vinal, G.W. (1955 Jan 01) Storage batteries. A general treatise on the physics and chemistry of secondary batteries and their engineering applications. Energy Citations Database (ECD) : Document #7308501
- John McGavack. The Absorption of Sulfur Dioxide by the Gel of Silicic Acid. Eschenbach Print. Company, 1920.
Patents
[edit]- U.S. patent 417,392 – Treatment Of Porous Pots For Electric Batteries. Erhard Ludwig Mayer and Henry Liepmann
- U.S. patent 3,271,199 – Solid Acid Storage Battery Electrolyte. Alexander Koenig et al.
- U.S. patent 4,134,192 – Composite battery plate grid
- U.S. patent 4,238,557 – Lead acid battery plate with starch coated glass fibers
- U.S. patent 4,414,302 – Method of making a lead storage battery and lead storage battery made according to this method. Otto Jache's and Heinz Schroeder
External links
[edit]- Why do I need a special battery for the automatic start-stop system?, published by Varta
- Pros and cons of AGM batteries, published by Lifeline
VRLA battery
View on GrokipediaHistory and Development
Invention and Early Milestones
The invention of the valve-regulated lead-acid (VRLA) battery began with the development of the gel electrolyte variant in 1957 by Otto Jache at the German company Sonnenschein. Jache's innovation involved mixing sulfuric acid with fumed silica to create an immobilized gel electrolyte, which prevented spills and enabled a sealed design while facilitating oxygen recombination to minimize water loss. This marked the first practical VRLA battery, patented and entering production that same year under the "dryfit" name, addressing key limitations of traditional flooded lead-acid batteries such as electrolyte leakage and maintenance needs.[4] In the 1960s and 1970s, further advancements focused on alternative immobilization methods, leading to the absorbent glass mat (AGM) design. The Gates Rubber Corporation initiated research in 1965, culminating in the first AGM prototype, known as the Cyclon cell, filed in 1972 and granted in 1975 by inventors John L. Devitt and Donald H. McClelland (US Patent 3,862,861). This spiral-wound cell used thin lead foil electrodes separated by a highly porous glass mat that absorbed the electrolyte, creating a starved system for efficient gas recombination without free liquid acid. Early prototypes underwent extensive testing, with licensing agreements like Sonnenschein's 1965 deal with Globe Union (Johnson Controls Inc.) accelerating global development.[5][3] Initial challenges in these developments centered on achieving reliable oxygen recombination efficiency and designing valves to manage internal pressure without compromising seal integrity. In gel designs, early rubber umbrella valves allowed gas venting but struggled with consistent recombination, leading to gradual water loss and overpressure risks during overcharge. AGM prototypes faced similar issues, including separator material failures (e.g., inadequate porosity in cellulose alternatives) and grid corrosion that reduced cycle life to mere hundreds of cycles. These hurdles required iterative improvements in electrolyte saturation and valve mechanisms to ensure safe, maintenance-free operation under varying temperatures and loads.[6][7] The first commercial introductions of VRLA batteries occurred in the late 1970s, primarily for demanding military and telecommunications applications where reliability and minimal maintenance were critical. Sonnenschein's gel cells found early use in portable military equipment and telecom backups, while VRLA cells supplied by Chloride entered trials with British Telecom in 1978–1979, paving the way for scaled production by 1983. These deployments highlighted VRLA's advantages in vibration-resistant, spill-proof power for remote or harsh environments.[3][8]Modern Advancements and Standardization
In the 1980s and 1990s, VRLA battery technology saw significant enhancements in separator materials and recombinant gas technology, enabling more efficient oxygen recombination and reducing water loss. Companies like Yuasa pioneered advanced microporous polyethylene separators that improved ionic conductivity while minimizing short-circuit risks, contributing to longer service life in sealed designs. Similarly, East Penn Manufacturing developed recombinant valve systems that optimized gas diffusion, allowing VRLA batteries to operate maintenance-free under deeper discharge cycles, which was crucial for emerging telecommunications applications. Standardization efforts in the 1990s formalized VRLA performance criteria, with the International Electrotechnical Commission (IEC) publishing the 60896 series for stationary applications, specifying requirements for capacity, endurance, and safety in valve-regulated lead-acid batteries. For automotive uses, the Japanese Industrial Standards (JIS) D 5301 established guidelines for VRLA reliability in starting-lighting-ignition (SLI) systems, ensuring consistent manufacturing and testing protocols across global markets. These standards facilitated widespread industry adoption by providing benchmarks for quality and interoperability. By the 2000s, VRLA batteries benefited from advancements in enhanced cycle life, particularly for renewable energy storage, where additives like carbon and lignosulfonate improved charge acceptance and reduced sulfation in photovoltaic systems. Integration with lithium-ion alternatives in hybrid energy storage systems emerged in the 2010s, allowing VRLA units to handle peak loads while lithium components managed high-discharge needs, as demonstrated in grid-scale projects. A key milestone in the 1990s was the broad adoption of VRLA in uninterruptible power supply (UPS) systems for data centers, where their reliability supported the IT boom. In the 2010s, improvements in high-temperature performance, such as heat-resistant alloys in grids, extended operational viability in harsh environments like solar farms in desert regions. Up to 2025, ongoing refinements focus on sustainability, including recyclable lead formulations that maintain over 1,000 cycles at 80% depth of discharge for off-grid applications.Operating Principles
Electrochemical Fundamentals
VRLA (valve-regulated lead-acid) batteries operate on the fundamental electrochemistry of lead-acid systems, where energy storage and release occur through reversible reactions between lead-based electrodes and sulfuric acid electrolyte. During discharge, the negative electrode (lead, Pb) and positive electrode (lead dioxide, PbO₂) react with sulfuric acid (H₂SO₄) to form lead sulfate (PbSO₄) and water (H₂O), releasing electrical energy. The overall discharge reaction is: This process consumes the active materials on both electrodes and dilutes the electrolyte. Charging reverses this reaction, reforming Pb and PbO₂ while regenerating H₂SO₄, with the overall charge reaction being the inverse of the discharge equation. These reactions occur at a nominal cell voltage of approximately 2 V, enabling common configurations such as 6 V (three cells) or 12 V (six cells) packs for practical applications.[9] A key feature distinguishing VRLA batteries from traditional flooded lead-acid designs is the immobilization of the sulfuric acid electrolyte, which prevents free liquid flow while preserving ionic conductivity essential for the reactions. In VRLA systems, the electrolyte is either absorbed into a glass mat separator or gelled with silica additives, maintaining a fixed structure that supports ion transport (primarily H⁺ and HSO₄⁻) between electrodes without spilling or stratification. This immobilization ensures consistent electrochemical performance under varying orientations and reduces internal resistance, allowing efficient charge-discharge cycling.[9][10] To minimize water loss and enable maintenance-free operation, VRLA batteries incorporate an oxygen recombination cycle during overcharge. At the positive electrode, excess charge generates oxygen gas via the reaction 2H₂O → O₂ + 4H⁺ + 4e⁻. This oxygen diffuses through the immobilized electrolyte to the negative electrode, where it recombines with lead and sulfuric acid: O₂ + 2Pb + 2H₂SO₄ → 2PbSO₄ + 2H₂O + heat. This cycle suppresses hydrogen evolution at the negative electrode, conserving electrolyte and enhancing safety. The energy efficiency of VRLA batteries, typically ranging from 70% to 85% (energy efficiency) and around 85% (coulombic efficiency), reflects the losses from overcharge and recombination processes.[9][11]Valve Regulation and Recombination
Valve regulation in VRLA batteries employs low-pressure relief valves that open at typically 2-10 psi to vent excess gases during overcharge, while under normal conditions, these valves remain closed to facilitate internal gas recombination and maintain the battery's sealed design. These self-resealing valves prevent external air ingress, which could lead to self-discharge or contamination of the electrolyte.[12] The recombination mechanism relies on oxygen generated at the positive electrode during overcharge—through the reaction 2H₂O → O₂ + 4H⁺ + 4e⁻—diffusing via the gas phase through the porous separator and thin electrolyte films to the negative electrode. There, it recombines with sponge lead in the presence of hydrogen ions and electrons to form water: O₂ + 4H⁺ + 4e⁻ → 2H₂O, effectively suppressing hydrogen evolution at the negative plate. This diffusion-driven process, enabled by the high-porosity separator (often >90% in AGM designs), ensures that internal pressure remains balanced during float charging.[13] In well-designed VRLA batteries, recombination efficiency reaches 95-99%, drastically reducing water loss and enabling long-term sealed operation without maintenance. By limiting hydrogen gas production and accumulation, this system enhances safety by minimizing the potential for explosive gas buildup within the battery enclosure.[14][13]Construction and Components
Core Structural Elements
The core structural elements of a valve-regulated lead-acid (VRLA) battery form a sealed, maintenance-free system designed for reliable energy storage and delivery. These components include the electrode plates, separators, housing, and terminals, which are assembled into individual cells and interconnected to achieve the desired voltage and capacity. This construction ensures structural integrity, electrical connectivity, and protection against environmental factors, while supporting the battery's valved regulation mechanism.[15][16] The plates serve as the primary electrodes, consisting of lead alloy grids coated with active materials. Negative plates feature a grid typically made of lead-calcium alloy filled with spongy metallic lead (Pb), while positive plates use a similar grid pasted with lead dioxide (PbO₂). The grids provide mechanical support and conductivity, and the active materials are applied as a paste of lead oxides mixed with additives, followed by a formation process where the battery undergoes an initial charge to electrochemically convert the paste into the functional Pb and PbO₂ layers. This design enhances durability and minimizes shedding of active material during cycling.[15][16][17] Separators vary by VRLA type and are inserted between positive and negative plates to prevent physical contact and short circuits while permitting ionic conduction. In gel batteries, they are thin, microporous sheets made of polyethylene or similar polymers, with pore sizes on the order of micrometers to balance ion permeability and mechanical strength. In AGM batteries, they consist of absorbent glass mats made from fiberglass, which provide electrical isolation, structural spacing, and electrolyte immobilization.[15][16] The battery case is constructed from flame-retardant acrylonitrile butadiene styrene (ABS) plastic, which offers high impact resistance, acid tolerance, and compliance with standards like UL 94 V-0 for fire safety. Terminals are integrated into the cover, commonly featuring threaded posts (e.g., M5, M6, or M8 sizes) or flag-style connectors (e.g., Faston 250) made of lead-electroplated copper to resist corrosion and facilitate series or parallel connections in battery banks. These elements ensure safe handling and electrical interfacing.[16][17] Assembly begins with grouping alternating positive and negative plates sandwiched by separators to form plate stacks, or "elements," for each cell. These stacks are inserted into the partitioned ABS case, with inter-cell connectors linking adjacent cells via lead-alloy straps burned or welded in place. The cover is then affixed using epoxy adhesive or heat-sealing techniques to create an airtight enclosure, preventing leaks and incorporating pressure-relief valves at designated points. This process yields a robust, sealed unit ready for electrolyte addition and final formation.[15][16][17]Electrolyte Containment Methods
In VRLA batteries, the sulfuric acid electrolyte, with a specific gravity of approximately 1.28 in the fully charged state, is immobilized to prevent free liquid flow that could lead to spills, while ensuring continuous ionic contact between the electrolyte and the electrode plates.[18] This containment strategy supports the battery's spill-proof design and enables operation in non-upright positions without compromising electrochemical performance.[15] The primary methods for electrolyte immobilization involve absorption into a porous medium or gelation, both of which restrict electrolyte mobility under gravitational forces or mechanical vibrations.[15] These approaches maintain electrolyte integrity by preventing settling or separation, thereby minimizing risks such as acid stratification where denser acid concentrates at the bottom of the cell.[15] Sealing techniques in VRLA batteries focus on creating a controlled internal environment, typically using pressure-relief valves integrated into sealed casings to allow excess gas venting while preserving the pressure required for oxygen recombination. Case assemblies often incorporate gaskets or welded joints to ensure airtight integrity around terminals and enclosures, preventing external contamination or electrolyte loss.[19] Quality control measures emphasize uniform electrolyte distribution to avoid localized dry-out or uneven concentration gradients that could accelerate degradation.[15] Manufacturers employ multi-stage filling and vacuum processes during assembly to achieve consistent saturation across plates and separators, with ongoing monitoring of specific gravity and fill levels to verify homogeneity.[15]Types of VRLA Batteries
Absorbent Glass Mat (AGM) Design
The Absorbent Glass Mat (AGM) design in VRLA batteries employs a separator composed of borosilicate glass microfiber mat, typically 20-30 μm thick, which serves to immobilize the electrolyte while facilitating ionic conduction between the positive and negative plates. This mat, made from fine borosilicate glass fibers with diameters ranging from 0.4 to 3 μm, exhibits high porosity—often exceeding 90%—enabling it to absorb and retain the sulfuric acid electrolyte entirely through capillary action, preventing any free liquid from forming. This full absorption, achieving up to 100% saturation of the electrolyte within the mat's structure, enhances the battery's spill-proof nature and supports efficient oxygen recombination during charging, a key feature of VRLA technology.[20][21][22][23] In the manufacturing process, the AGM separator is integrated during plate assembly, where the glass mat is placed between the lead-based positive and negative plates to form cell elements. Following assembly, the electrolyte is injected into the sealed battery case under vacuum conditions to ensure even distribution, after which the mat is compressed—typically to 10-20 kPa—to achieve 90-95% saturation without excess free acid, optimizing contact between the electrolyte and active materials. This compression step minimizes internal resistance and prevents plate separation over time, contributing to the battery's structural integrity. The resulting design allows for recombinant operation, where gases generated during overcharge are reabsorbed, reducing water loss.[15][24][25] AGM batteries offer distinct performance advantages, including superior vibration resistance due to the tightly packed, immobilized components that withstand mechanical stresses better than flooded designs, making them ideal for automotive and marine applications. In particular, AGM batteries are the top choice for marine use in outboard motors because they are sealed, highly vibration-resistant, spill-proof, and low-maintenance—ideal for the demanding boating environment.[26][27][28] They generally provide higher cold cranking amps (CCA) compared to flooded lead-acid batteries, offering better starting performance in cold weather conditions where flooded batteries may struggle. AGM batteries also tend to have a longer lifespan in demanding applications due to reduced sulfation and better resistance to temperature extremes. They support fast discharge rates up to 10C, enabling high-power delivery for starting or inverter loads, and provide deep cycle capability of 500-1000 cycles at 50% depth of discharge (DOD), extending service life in cyclic uses. With a typical specific power density of 150-200 W/kg, AGM configurations excel in high-drain scenarios such as uninterruptible power supplies (UPS) and electric vehicles, where rapid energy release is critical.[29][30][31][32][33][30][34][35]Gel Electrolyte Design
The gel electrolyte in VRLA batteries is formed by mixing sulfuric acid with 2-5% fumed silica, creating a semi-solid, immobilized paste that maintains structural integrity and prevents electrolyte stratification.[36][37] This composition renders the battery spill-proof, as the gel holds the electrolyte in place even if the casing is cracked or damaged.[38][39] In manufacturing, the gel is typically formed in situ after assembling the cell with pre-formed positive and negative plates; the liquid mixture of sulfuric acid and fumed silica is introduced into the cell, where it cures into a gel during the initial conditioning process.[40] Pre-forming the plates externally avoids excessive gassing within the sealed cell, which could otherwise disrupt the gel structure or cause pressure buildup.[41] This approach ensures uniform electrolyte distribution and enhances long-term stability without requiring post-assembly formation charging inside the battery. Gel electrolyte designs offer excellent deep cycle performance, typically achieving 500-1000 cycles at 50% depth of discharge (DOD), due to the immobilized electrolyte's ability to support repeated deep discharges without significant active material degradation.[42] They also demonstrate better tolerance to overcharge compared to AGM variants, as the gel reduces the risk of dry-out from electrolyte loss during excessive charging.[43] Additionally, these batteries exhibit low self-discharge rates of 1-3% per month at ambient temperatures, making them suitable for applications with infrequent use.[44] Despite these strengths, gel electrolyte VRLA batteries have slower charge acceptance rates owing to the higher internal resistance of the gel, which limits rapid recharging compared to more fluid electrolyte systems.[45] They also provide reduced cold cranking amps (CCA), as the viscous gel impedes ion mobility at low temperatures, resulting in lower power output for high-demand starting applications relative to AGM designs.[46][43]Key Differences Between AGM and Gel
Absorbed Glass Mat (AGM) and gel batteries represent two primary subtypes of Valve-Regulated Lead-Acid (VRLA) batteries, differing fundamentally in electrolyte immobilization and resulting performance characteristics. AGM batteries use a fiberglass mat to absorb the sulfuric acid electrolyte, enabling higher power output and better suitability for demanding applications, while gel batteries incorporate silica to form a semisolid electrolyte, prioritizing stability and longevity in sustained use.[47][48] In terms of performance, AGM batteries excel at high-rate discharges, delivering peak currents such as 200-500 cold cranking amps (CCA) for short bursts, making them ideal for engine starting or high-load scenarios where rapid power delivery is critical.[48][30] In contrast, gel batteries provide steady, low-rate output optimized for deep-cycle applications, with lower internal resistance allowing consistent performance over extended periods but limiting their capability for high-current demands. Regarding temperature tolerance, gel batteries handle extremes more robustly, operating effectively from -40°C to 60°C due to the immobilized electrolyte's resistance to stratification and freezing, whereas AGM batteries perform better in cold conditions below 0°C but may degrade faster in prolonged high heat.[49][23] Cost and lifespan vary based on usage patterns. AGM batteries are typically 20-30% more expensive upfront due to their advanced construction, but they offer shorter longevity in float service (around 6-10 years) compared to gel's extended durability in similar standby roles. In cyclic applications, however, gel batteries prove cheaper long-term, achieving 500-1000 cycles at 50% depth of discharge (DOD) versus AGM's 500-1000 cycles, thanks to reduced electrode wear and better recombination efficiency.[50][51][42] Suitability aligns with these traits: AGM batteries are preferred for starting, lighting, and ignition (SLI) systems in vehicles and marine outboard motors, where high instantaneous power and vibration resistance are essential, while gel batteries suit solar photovoltaic backups and inverters, leveraging their deep-cycle endurance and low self-discharge for reliable, maintenance-free operation in off-grid setups.[47][48]| Metric | AGM | Gel |
|---|---|---|
| Energy Density (Wh/kg) | 30-40 | 25-35 |
| Cycle Life (at 50% DOD) | 500-1000 cycles | 500-1000 cycles |
| Temperature Range (°C) | -20 to 50 (optimal) | -40 to 60 |
| Peak Discharge (e.g., CCA) | 200-500 A | <200 A (low-rate focus) |