| HS Code | 336654 |
| Electrolyte Type | Organic |
| Solvent | Acetonitrile (ACN) |
| Supporting Salt | Tetraethylammonium tetrafluoroborate (TEABF4) |
| Salt Concentration | 1.0 M |
| Ionic Conductivity | 20 mS/cm at 25°C |
| Voltage Window | 0–2.7 V |
| Operating Temperature Range | -40°C to +70°C |
| Electrochemical Stability | Stable up to 3.0 V |
| Viscosity | 0.6 cP at 25°C |
| Specific Gravity | 0.78 g/cm³ at 25°C |
| Flammability | Flammable |
| Typical Capacitance Retention | >90% after 1000 cycles |
As an accredited Conventional Electrolyte for EDLC factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Conventional Electrolyte for EDLC supplied in 1 L sealed HDPE bottle, stored under inert atmosphere. |
| Container Loading (20′ FCL) | 20′ FCL: Conventional Electrolyte for EDLC securely packed in drums, labeled, ventilated, and containerized for safe transport. |
| Shipping | Ship as a flammable, toxic liquid. Use UN-approved containers with corrosion-resistant liners, secure against leaks and static discharge. Label with proper hazard class, keep away from oxidizers and moisture, and ensure temperature-controlled transport. Include SDS and follow all relevant international, maritime, and road freight regulations for electrolyte solutions. |
| Storage | Store in tightly sealed, moisture-proof containers under a dry, cool, well-ventilated area, ideally under inert gas. Protect from direct sunlight, heat, and ignition sources. Keep away from water, oxidizing agents, and incompatible materials. Follow manufacturer’s guidelines; avoid prolonged exposure to air to maintain electrolyte purity and performance. |
| Shelf Life | Shelf life typically 24 months when stored sealed, dry, and at room temperature, protected from moisture and direct sunlight. |
Conventional electrolyte for electric double-layer capacitors is supplied as a ready-to-fill non-aqueous solution of tetraethylammonium tetrafluoroborate in acetonitrile or propylene carbonate. The acetonitrile grade carries a salt concentration of 1.0 mol/L, bulk conductivity at 25 °C of 55–60 mS/cm, water content ≤20 µg/g, and free acidity expressed as HF ≤15 µg/g. The propylene carbonate grade is specified at 1.0 mol/L, 13–15 mS/cm, and water content ≤30 µg/g. The electrolyte is introduced after electrode winding or stacking, before terminal welding and formation. It is not a slurry additive and is not intended for lithium-ion cells, lithium-ion hybrid capacitors with intercalation anodes, or aqueous EDLC systems. Dedicated filling equipment is required; shared use with lithium-ion electrolyte lines must be prevented because residual lithium hexafluorophosphate or carbonate solvents can destabilize the tetrafluoroborate salt and shift cell ESR. Free water, uncoated copper, and amine-based additives are incompatible with this electrolyte family.
| Electrolyte grade | Conductivity at 25 °C | Water ceiling | Operational temperature window |
|---|---|---|---|
| Acetonitrile conventional | 55–60 mS/cm | ≤20 µg/g | −40 °C to +60 °C |
| Propylene carbonate conventional | 13–15 mS/cm | ≤30 µg/g | −25 °C to +70 °C |
In 48 V mild-hybrid electrical architectures, the EDLC module sits parallel to the DC-DC converter or belt starter generator to absorb recuperation current peaks and supply cold-cranking support after a stop phase. The conventional electrolyte selected for this route is the acetonitrile grade because its bulk ionic conductivity at −40 °C remains sufficiently high to limit module DC ESR below the board-level acceptance threshold set by the automaker. Unlike backup applications, this service is dominated by continuous partial-state charge cycling at a cell voltage window of 1.5 V to 2.7 V and pack-level RMS currents that can exceed 300 A during active anti-roll bar actuation. The electrolyte must therefore tolerate frequent micro-cycling without accumulating solvent decomposition products at the activated carbon surface; moisture ingress and free acidity are the two lot-release variables most tightly controlled by the cell manufacturer.
Cell-level qualification for automotive EDLCs follows IEC 62391-2:2019 for endurance and humidity load, while module-level electrical testing follows ISO 16750-2:2018 for 48 V transient overvoltage and supply dip with start-stop profile. Passive-component environmental stress is checked according to AEC-Q200 Rev D, specifically high-temperature exposure at 85 °C and thermal shock from −40 °C to 85 °C. The electrolyte lot must be released with water ≤20 µg/g, free acidity expressed as HF ≤15 µg/g, and chloride ≤2 µg/g to limit aluminum current collector pitting during the 10-year vehicle life. The addition ratio is calculated from the combined mercury-intrusion pore volume of the positive electrode, negative electrode, and separator, plus a 8–12% excess to accommodate terminal wetting and header void space. For wound cylindrical cells with calendered activated-carbon coatings of 200–220 µm thickness and 55–60% porosity, this corresponds to an electrolyte-to-dry-carbon mass ratio of 2.0:1 to 2.3:1.
Downstream cell production begins with high-shear dispersion of activated carbon, conductive carbon black, and binder in aqueous or solvent slurry; the coating is applied to etched aluminum foil, dried, calendered, slit, and wound with a cellulosic separator on cylindrical winders. Electrolyte is introduced on a vacuum filling carousel at −0.09 MPa to −0.10 MPa cell internal pressure, followed by constant-current formation to 2.7 V at a rate not exceeding 1C, then aging at 65 °C for 24 h, pressure release, and laser welding of the overpressure vent. Module assembly applies cell-to-cell clamping at 0.3–0.5 MPa to control ESR growth and uses laser-welded busbar interconnects before conformal coating and end-of-line testing. Terminal products are 16 V 58 F, 16 V 100 F, and 48 V 165 F EDLC modules used in 12 V/48 V stop-start systems, electric compressor peak power buffers, active chassis stabilizer control, and emergency door latch release after a crash. In each case the module is hardwired to the battery rail through a bidirectional DC-DC converter, not directly across the alternator output.
Propylene carbonate replaces acetonitrile in utility meter backup because the sealed PCB-mount device is subjected to enclosure temperatures of 70 °C or higher for days in direct sunlight, and the closed-cup flash point of acetonitrile is 2 °C. The low vapor pressure of propylene carbonate reduces case bulging and electrolyte creep across the elastomer seal during the 15-year service interval required by metering operators. The penalty is lower ionic conductivity, but the discharge load for a real-time clock and communication flag is typically below 10 mA, so the −20 °C conductivity of the PC grade remains adequate for the 2 s to 30 s bridge duration. Metering-grade cells therefore prioritize seal stability and leakage current over milliohm impedance, which is the inverse of the automotive or rail design hierarchy.
Metering-grade EDLC cells are qualified under IEC 62391-1:2015 for fixed general-purpose electric double-layer capacitors and under IEC 62052-11:2020 for electricity metering equipment with respect to environmental endurance. North American product listings typically require UL 810A recognition for electrochemical capacitors. The formulation fill ratio for thin-electrode radial cells is held at 1.5:1 to 1.8:1 electrolyte-to-dry-carbon mass. The lower bound reduces excessive free electrolyte that would otherwise contribute to leakage current and seal wetting; the upper bound is set by the need to maintain 90% rated capacitance after 1,000 h at 70 °C under 2.5 V applied bias.
Downstream production uses high-speed radial taping lines with automated electrolyte dosing needles, crimp sealing, and two-stage aging under temperature. Process control focuses on dew point in the assembly room, which is maintained at ≤−30 °C for PC-grade cells because the electrolyte is hygroscopic and free water hydrolyzes tetraethylammonium tetrafluoroborate into HF. Finished terminal products are 5.5 V 0.22 F, 5.5 V 0.47 F, and 5.5 V 1.0 F PCB-mount EDLCs used for automatic meter reading communication, last-gasp data retention, and valve shut-off actuation in smart gas and water meters.
Cold-start discharge at −40 °C is the primary sizing constraint for wind turbine pitch-control backup. A loss of grid power requires the pitch motor to move blades to feather within 20 s to 60 s, drawing high current from an unconditioned nacelle enclosure. The acetonitrile-based conventional electrolyte is specified because its bulk conductivity at −40 °C remains near 28 mS/cm, whereas propylene carbonate drops below 5 mS/cm. This difference translates directly into lower ESR and less voltage droop during the first seconds of discharge, which is decisive when the pitch motor inrush current coincides with cold hydraulic oil and high blade loading.
Turbine electrical backup modules are validated against IEC 61400-1:2019 for wind turbine generator systems and IEC 62391-2:2019 for power-type fixed EDLC endurance. The electrolyte handling and assembly line must comply with acetonitrile vapor exposure limits and ATEX zoning because the solvent has a closed-cup flash point of 2 °C and a lower explosion limit of 3.0 vol%. For large cylindrical cells of 3000 F with electrode thickness of 300–350 µm, the electrolyte-to-dry-carbon ratio is set at 2.2:1 to 2.4:1. The higher ratio compensates for the longer wetting path in deeply coated electrodes and for the low-temperature viscosity increase of acetonitrile.
Downstream production winds the cell elements under tension, welds the aluminum current collector tabs by ultrasonic welding, and transfers the cells into a vacuum filling station purged with dry nitrogen at a dew point of ≤−40 °C. After electrolyte filling, the cell is held under 0.05 MPa nitrogen overpressure to force electrolyte into the electrode pores, then electrically formed to 2.7 V and aged at 60 °C for 72 h. Cells are sorted by ESR and capacitance into matched sets before module stacking. Terminal products are battery-free pitch-control backup modules rated 16 V / 500 F, 24 V / 125 F, and 48 V / 83 F that replace VRLA batteries in the nacelle. The operational boundary is that these modules are sealed and vent-only under fault conditions; acetonitrile should not be handled in open containers inside the nacelle without forced ventilation and continuous lower-explosion-limit monitoring.
Fast-charge automated guided vehicles and reach stackers impose a different stress on the electrolyte: unlike long-hold backup, this route is dominated by continuous partial-state charge cycling at 100 A to 400 A pack level and opportunity charging at rates that bring the cell from 50% to 90% state of charge in 60 s to 120 s. The acetonitrile-based conventional electrolyte is selected because of its 55–60 mS/cm conductivity at 25 °C, which minimizes resistive heating between cell terminals and the aluminum current collector tabs. Failure analysis of returned AGV modules has shown that connector and busbar hotspots, not electrolyte conductivity, become the limiting factor above 5C continuous discharge, so the electrolyte acceptance window focuses on water and acidity rather than ultra-high conductivity grading.
Module safety and performance are qualified under IEC 62391-2:2019 for power-type fixed EDLCs and the vehicle-level functional safety requirement is addressed through ISO 3691-4:2020 for driverless industrial trucks. Workplace electrical conformity follows IEC 60204-1:2016 for electrical equipment of industrial machines, specifically the short-circuit and residual-voltage discharge requirements that dictate passive discharge resistors across each module. The electrolyte-to-dry-carbon mass ratio is set at 1.8:1 to 2.1:1 for pouch and cylindrical cells with 180–250 µm electrodes. The addition ratio is selected on the lower side of the range to reduce excess free liquid that can migrate during constant AGV vibration and accumulate at the seal shoulder.
Downstream production uses automatic stacking or winding, followed by dry-room filling at −50 °C dew point, formation at 2.7 V, and a 72 h voltage-hold step to reject cells with hidden separator debris or incomplete wetting. Modules are assembled with active cell balancing boards set to clamp at 2.65 V/cell and passive discharge resistors that bring the floating bus below 60 V DC within 5 s after maintenance disconnect. The operational boundary is strict: continuous charge above 2.85 V/cell at room temperature initiates solvent decomposition and gas generation, so the balancer must never allow the string midpoint to drift beyond 2.65 V/cell. Terminal products are 24 V / 300 F, 48 V / 165 F, and 80 V / 125 F capacitor banks used for AGV opportunity charging, port straddle carrier peak shaving, and regenerative braking capture in empty container handlers. The capacitor bank is paralleled to a small lithium iron phosphate battery that supplies standby electronics; the EDLC handles the high-frequency charge-discharge component.
Data center UPS bridge power uses EDLC banks to cover the 10 s to 30 s generator start window rather than long-term backup. The conventional electrolyte for indoor rack-mounted modules is propylene carbonate where fire code jurisdiction limits solvent volatility. The PC grade reduces electrolyte vapor pressure and simplifies indoor code documentation, at the cost of higher ESR than the acetonitrile grade, but the short discharge window does not require milliohm-level pack impedance. The service profile is float-heavy and cycle-light, so electrolyte stability under constant polarization becomes more important than low-temperature power delivery.
UPS interface compatibility is qualified under IEC 62040-3:2021 for uninterruptible power system performance and UL 1778:2016 for safety of power converters and UPS. For battery-room and data-hall deployment, installation follows NFPA 855:2020 energy storage system requirements where the local authority having jurisdiction classifies the EDLC bank as stationary energy storage. The electrolyte itself is specified with free fluoride ≤15 µg/g and sulfate ≤5 µg/g to avoid slow internal corrosion of the aluminum tab surface over a 10-year stationary life. The electrolyte-to-dry-carbon ratio is set at 1.6:1 to 2.0:1 for large prismatic modules with 150–200 µm electrodes; the lower bound is used to reduce self-discharge and leakage current because a data center UPS sits at float for months and is not cycled daily.
Downstream production fills individual cells under vacuum, then mounts the cells in 19-inch rack-mountable trays with busbar connections torqued to 8–10 N·m and monitored by cell voltage supervisors. After assembly, the complete rack bank undergoes a 48 h float test at 2.65 V/cell with thermal imaging to identify interconnector defects before shipment. Terminal products are 48 V / 83 F and 48 V / 166 F rack-mount EDLC modules placed between the AC-DC rectifier and the generator transfer switch, as well as 400 V series strings for three-phase UPS ride-through in colocation facilities. The modules are current-limited and fused on each cell group to prevent cascading failure in a short-circuit event.
When a light-rail vehicle decelerates into a station, the traction converter reverses power flow and the on-board or wayside capacitor bank must accept a charge pulse that batteries cannot absorb without lithium plating or thermal derating. The acetonitrile-based conventional electrolyte is specified for this service because the charge pulses are high-rate and repetitive, requiring low ionic resistance at 25 °C and minimal concentration polarization during 10 s to 20 s braking events. The rail environment also imposes continuous vibration and a wide ambient temperature envelope from −25 °C to +55 °C within the equipment cabinet, so the electrolyte must remain within its electrochemical stability window across the full climatic profile without cell venting.
Rail vehicle electronic equipment qualification follows EN 50155:2021 for electronic equipment used on rolling stock and EN 61373:2010 for vibration and shock testing. Capacitor-specific traction applications are addressed by IEC 61881-3:2018 where applicable to power electronics capacitors, supplemented by fire-safety evidence under EN 45545-2:2013 for passenger rolling stock. The sealed EDLC cells must demonstrate no electrolyte leakage after the specified vibration profile and must remain below the referenced toxicity index for organic solvent vapors during a simulated fault. For roof-mounted capacitor cabinets, the electrolyte-to-dry-carbon mass ratio is set at 2.2:1 to 2.5:1, the upper end driven by large 3000 F cells with thick electrodes and by the need to maintain capacitance balance across long series strings.
Downstream production winds, fills, and forms the cells as high-power cylindrical EDLCs, then assembles them into series strings with active voltage balancing at 2.55 V/cell to 2.65 V/cell. The cabinet includes pressure-equalization ports with hydrophobic membranes, forced-air cooling for tunnels, and cell-level fusing. Published data for the exact lower-explosion-limit dispersion profile of acetonitrile from a single vented 3000 F cell is limited; cabinet suppliers therefore apply computational fluid dynamics with the solvent lower explosion limit of 3.0 vol% as the acceptance threshold. Terminal products are roof-mounted 125 V / 167 F and 750 V / 28 F braking energy recovery modules, as well as station fast-charge capacitor banks for catenary-free segments. The EDLC bank is controlled by a bidirectional DC-DC converter that limits charge voltage to the continuous rated voltage and returns stored energy during acceleration; no separate lithium-ion pack is required.
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Product designation AN-TEABF4-1M is a conventional electrolyte for electric double-layer capacitors (EDLCs), supplied as a 1 mol L−1 solution of tetraethylammonium tetrafluoroborate (TEABF4) in anhydrous acetonitrile. The model designation encodes the solvent system, salt chemistry, and molar concentration: AN denotes acetonitrile, TEABF4 identifies the quaternary ammonium salt, and 1M specifies the concentration. In commercial EDLC cells, the electrolyte functions as the ionic conductor that charges the porous carbon electrode/electrolyte double layer; it does not participate in faradaic charge transfer under normal operation. The liquid is clear and near-colourless, with a typical conductivity of 55–65 mS cm−1 at 25 °C and a coulometric water specificationnot exceeding 20 mg kg−1. Equivalent commercial grades with the same composition appear under supplier-specific trade names, but the AN-TEABF4-1M designation identifies the conventional solvent-salt system used across radial, cylindrical, and pouch EDLC platforms.
Incoming electrolyte is released against conductivity, water content, density, viscosity, and visual clarity because these parameters control initial equivalent series resistance, formation behaviour, and long-term gas evolution. Moisture above 20 mg kg−1 is rejected for cells rated at 2.7 V; water adsorbed on the activated carbon surface participates in anodic oxidation and hydrogen evolution during formation, producing irreversible capacitance loss and internal pressure rise. Conductivity is measured with a calibrated conductivity cell having an accuracy of 0.5 %, and the measurement temperature is held at 25.0 ± 0.1 °C. Conductivity shows a temperature coefficient of approximately 1.5–2.0 % per °C near room temperature, so fill-line measurements made at 20 °C or 30 °C must be corrected before release. Water content is determined by Karl Fischer coulometry according to ASTM E1064, density by ASTM D4052, kinematic viscosity by ASTM D445, and solvent flash point by ASTM D3278. The solvent is acetonitrile with a purity of at least 99.9 % by gas chromatography, because residual propionitrile, acrylonitrile, or water alters double-layer capacitance and leakage current.
| Property | Test method | Numerical acceptance range |
|---|---|---|
| Conductivity at 25 °C | Calibrated conductivity cell | 55–65 mS cm−1 |
| Water content | ASTM E1064 coulometric Karl Fischer | ≤ 20 mg kg−1 |
| Density at 20 °C | ASTM D4052 | 0.80–0.85 g cm−3 |
| Kinematic viscosity at 25 °C | ASTM D445 | ≤ 1.0 mm² s−1 |
| Acetonitrile purity | Gas chromatography–flame ionisation detection, supplier method | ≥ 99.9 % by area |
| Chloride | Anion chromatography after aqueous dilution | ≤ 5 mg kg−1 |
| Free fluoride | Ion-selective electrode after hydrolysis | ≤ 20 mg kg−1 |
| Appearance | Visual inspection against black/white background | Clear, no visible particulate |
On cylindrical and pouch EDLC assembly lines, the electrolyte is introduced after electrode drying under vacuum. Activated carbon electrodes with porosity of 0.40–0.60 and carbon loading of 5–12 mg cm−2 are typical for conventional acetonitrile systems. The filling chamber is evacuated to a residual pressure below 10 mbar before the product is dosed, and the fill volume is set to achieve complete wetting without excess free liquid. Electrolyte hold-up in the separator is generally 1.0–1.5 µL cm−2 per separator layer. Batch-to-batch conductivity variation on production packaging lines is commonly below ±0.5 mS cm−1; a larger shift indicates container leakage, moisture ingress, or salt decomposition. After filling, the cell headspace is purged with dry nitrogen and the cell is sealed. Formation charging is conducted under constant current at 1–5 mA cm−2 up to 2.5–2.7 V, followed by voltage hold at room temperature until the leakage current decays to a stable plateau.
The operational boundary at high voltage is dominated by anodic oxidation of acetonitrile and decomposition of TEABF4 on carbon surfaces. On a glassy carbon electrode, the onset potential for electrolyte oxidation is observed near 3.2 V versus Ag/Ag+, but porous activated carbon with high surface area and oxygen-containing edge sites lowers the practical cell limit to 2.7–2.85 V. At 2.85 V and 65 °C, accelerated gas generation has been observed in pouch cells with activated carbon electrodes. Published data for EDLC electrolytes with water contents intentionally raised to 50 mg kg−1 report capacitance fade exceeding 10 % after 1000 h float at 2.7 V. When the product meets the 20 mg kg−1 water limit, float performance at 2.7 V and 50 °C is typically stable for several thousand hours, but continuous operation above 70 °C is not recommended because acetonitrile vapour pressure and salt decomposition both accelerate. Endurance testing under IEC 62391-1:2022 at 2.7 V and 65 °C is used for verification. Voltage hold protocols after formation use leakage current criteria rather than time-only endpoints; a cell is considered stable when leakage current decays below 0.5 mA F−1 at 25 °C. The solvent is a flammable liquid with a closed-cup flash point of 2 °C; transfer and storage therefore require inert gas blanketing, explosion-proof electrical classification, and control of electrostatic discharge. Incompatibilities include strong oxidizing agents, strong mineral acids, halogens, and materials that catalyse acetonitrile decomposition. Seal compatibility must be verified because acetonitrile has higher solvent power than propylene carbonate and may swell nitrile elastomers or extract plasticisers from low-density polyolefins.
The choice between conventional AN-TEABF4-1M and a propylene carbonate-based electrolyte is driven by the trade-off between low-temperature resistance and high-temperature safety margin. AN-TEABF4-1M retains a conductivity above 30 mS cm−1 at −20 °C, whereas PC-based TEABF4 falls below 5 mS cm−1 under the same condition. This difference translates to a lower ESR rise in cold-cranking applications and automotive start-stop modules. Conversely, PC-based electrolytes offer a flash point above 130 °C and a boiling point above 240 °C, which simplifies thermal runaway containment and allows float operation at 80–85 °C when the salt system is designed for high temperature. Ionic liquid and spiro-salt systems extend the voltage window to 3.0–3.5 V but introduce higher viscosity, often 20–80 mPa·s, and lower conductivity, typically 5–15 mS cm−1. The comparative data are summarised below.
| Property | AN-TEABF4-1M | PC-TEABF4-1M | Ionic liquid or spiro-salt high-voltage system |
|---|---|---|---|
| Conductivity at 25 °C | 55–65 mS cm−1 | 12–15 mS cm−1 | 5–15 mS cm−1 |
| Viscosity at 25 °C | ≤ 1.0 mPa·s | 3–5 mPa·s | 20–80 mPa·s |
| Solvent flash point | 2 °C | 132 °C | Typically > 200 °C |
| Practical cell voltage | 2.7 V | 2.7 V | 3.0–3.5 V |
| Low-temperature limit before severe ESR rise | −40 °C | −20 °C | 0 to −10 °C |
| High-temperature continuous duty without derating | 50–60 °C | 70–85 °C | 80–100 °C |
For pack-level integration, AN-TEABF4-1M is specified when the cell voltage is limited to 2.5–2.7 V and the ambient operating temperature does not exceed 60 °C. The product is not specified for cells rated at 3.0 V unless the electrode is specifically stabilised for higher anodic potential; using AN-TEABF4-1M in a 3.0 V system without such stabilisation produces gas and internal pressure rise. The product is also unsuitable for continuous-duty solar, smart-meter, or backup-power applications requiring a 15-year life at 70 °C with zero maintenance; PC-based, ionic liquid, or spiro-salt systems have lower vapour pressure and higher thermal stability. In custom cell designs, published data for this specific configuration is limited, so qualification must include float testing at the maximum rated voltage and maximum rated temperature under IEC 62391-1:2022. The electrolyte should be stored in sealed stainless steel or fluoropolymer-lined containers under dry nitrogen, and open handling should be confined to a dry room with a dew point not higher than −40 °C.