DSS CQES2308000357BA UL9540Aı ¿© - 300ah
DSS CQES2308000357BA UL9540Aı ¿© - 300ah
DSS CQES2308000357BA UL9540Aı ¿© - 300ah
For
ANSI/CAN/UL9540A
Test Method for Evaluating Thermal Runaway Fire
Propagation in Battery Energy Storage Systems
[Cell Level]
Remark: Test results reported relate only to the items being tested.
Strictly Confidential
Remark: This report only evaluated cell level test which is listed inside the dotted box.
Model: 72173204
Manufacturer: Guangzhou Rongjie Energy Technology Co., Ltd
Nominal capacity: 300 Ah
Nominal voltage: 3.2 V
Chemistry: Lithium-ion, LiFePO4
Maximum charge power: 480 W
Maximum discharge power: 480 W
Maximum charge voltage: 3.85 V
Cut-off Voltage: 2.5 V (>0°C)
2.0 V (≤0°C)
Charge temperature range: 0 to 55 °C
Discharge temperature range: -20 to 55 °C
External dimensions: L×W×H = (71.7±0.5) mm × (174.6±0.5) mm × (207.1±0.6) mm
Weight: 5.7±0.3 kg
UL 1973 compliant: Yes / No N/A
Cell samples shall be conditioned, prior to testing, through charge and discharge cycles for a minimum of 2
cycles using a manufacturer specified methodology to verify that the cells are functional. Each cycle shall be
defined as a charge to 100% SOC and then to an end of discharge voltage (EODV) specified by the cell
manufacturer. During conditioning a relationship between open circuit voltage and SOC shall be determined
through measurement of voltage and SOC. During conditioning the ambient temperature shall be maintained
in accordance with the higher of 25 ±5°C or the operating temperature in the cell manufacturer's
specifications.
The cells to be tested shall be charged to 100% SOC and allowed to stabilize for a minimum of 1 h and a
maximum of 8 h before the start of the test.
Cells with flexible laminate casings shall be constrained during the test in the manner that simulates the
constraint in the BESS module to prevent excessive swelling during the test.
Ambient indoor laboratory conditions shall be 25 ±5°C (77 ±9°F) and 50 ±25% RH at the initiation of the test.
The propensity of the cell to exhibit thermal runaway shall be demonstrated by heating the cell with
externally applied flexible film heaters that cover as much of the cell case as possible without covering
safety features or terminals, for consistent heating of the internal cell electrode assembly. A surface heating
rate of 4°C (7.2°F) to 7°C (12.6°F) per minute shall be applied to the cell. Determination of a maximum
surface temperature end point criteria shall be developed based upon a review of cell design and chemistry.
Before beginning the test, a surface temperature shall be determined to approximate the temperature at
which internal short circuiting within the cell will occur that could lead to a thermal runaway condition. For Li-
ion cells, the surface temperature hold point shall be between 5°C (9°F) and 15°C (27°F) greater than the
melting temperature of the cell separator material as determined from differential scanning calorimetry (DSC)
data of the separator in accordance with UL 2591 (UL 746A). Thermal runaway may occur before this hold
point temperature range is reached. However, if thermal runaway is not achieved at this hold point
temperature after a period of 4 h, the cell heating rate of 4°C (7.2°F) to 7°C (12.6°F) per minute shall be
reestablished until thermal runaway occurs or it is demonstrated that thermal runaway is not achievable by
heating.
If the cell is susceptible to thermal runaway by external heating, the cell shall be heated until thermal
runaway has occurred. If the cell is not susceptible to thermal runaway by heating with a film heater, another
method shall be employed. If using another external heating method, the temperature ramp and maximum
surface temperature shall be used.
The cell's exterior surface temperature shall be measured continuously through the cell test with a
thermocouple junction formed from 24-gauge or smaller, Type-K thermocouple wire. The location(s) of
thermocouple (s) shall be determined during a construction review. At least one thermocouple shall be
located below the heater film at the center of the cell surface (if the cell is prismatic this would be the center
of the wider side of the cell) and one near the positive cell terminals.
The temperature at the onset of thermal runaway shall be documented. Onset of thermal runaway shall be
determined by the point at which the rate of change of the surface temperature of the cell exceeds that of
the externally applied heat input if utilizing the external heater method. Thermal runaway is a condition
where there is heating of the cell in an uncontrolled manner and should not be confused with overheating
leading to venting only. Cell venting may occur first, but it is necessary to continue heating when using the
heater method until thermal runaway occurs. With other stress methods, it will be necessary to continue
applying the stress such as mechanical or electrical stress until onset of thermal runaway occurs. If there is
a transitory temperature dip during the cell venting, the heat input may need to be increased to bring it back
to the heating rate range.
When using methods other than the heater method, the stresses (i.e. electrical or mechanical) shall be
applied to the cell until thermal runaway occurs. Thermal runaway is considered to have occurred,
regardless of the method of stress chosen, when there is a rapid increase in temperature and should not be
confused with simple overheating leading to venting.
If the cell exhibits thermal runaway behavior (using any method), 3 additional samples shall be tested using
the same method and exhibit thermal runaway to demonstrate repeatability. The vent temperature and
thermal runaway onset temperatures shall be averaged over the tested samples (excluding the gas vent
capture sample). This average temperature shall be used to establish the temperature limits for the other
test levels of this standard.
Cell vent gas shall be generated and captured by forcing a cell into thermal runaway with the methodology
developed in above, inside a pressure vessel, which is large enough to accommodate cells, but not so large
as to influence measurement of the gas composition. An 82-L (21.7-gal) pressure vessel is recommended
for this purpose for most sizes of commercially available cells. The test shall be initiated with an initial
condition of atmospheric pressure and less than 1% oxygen by volume. The initial atmospheric conditions
prior to testing shall be noted.
Cell vent gas composition shall be determined using Gas Chromatography (GC) with detection techniques
for quantifying component gases or equivalent gas analysis techniques, to identify hydrocarbon gases that
represent an ignition or explosion hazard as well as other additional gases requested to be measured.
Hydrogen gas shall be measured with a sensor capable of measuring in excess of 30% by volume. The
initial atmospheric conditions prior to testing shall be noted.
Upon determination of the cell vent gas composition, the lower flammability limit of the cell vent gas shall be
determined on samples of the synthetically replicated gas mixture in accordance with ASTM E918, testing at
both ambient and cell vent temperatures.
The synthetically replicated gas mixture shall be used to determine gas burning velocity in accordance with
the Method of Test for Burning Velocity Measurement of Flammable Gases Annex in ISO 817.
The synthetically replicated gas mixture shall be used to determine Pmax in accordance with EN 15967.
T8 Ambient temperature --
Thermocouple information:
Type K, 24AWG
Figure 4c. View of cell M1 during test_E3 Figure 4d. View of cell M1 during test_E4
Figure 4e. View 01 of cell M1 after test Figure 4f. View 02 of cell M1 after test
T8 Ambient temperature --
Thermocouple information:
Type K, 24AWG
Figure 6a. View 01 of cell M2 before test Figure 6b. View 02 of cell M2 before test
Figure 6c. View of cell M2 during test_E3 Figure 6d. View of cell M2 during test_E4
T5 -- --
T7 -- --
T8 Ambient temperature --
Thermocouple information:
Type K, 24AWG
Figure 8c. View of cell M3 during test_E3 Figure 8d. View of cell M3 during test_E4
Figure 8e. View 01 of cell M3 after test Figure 8f. View 02 of cell M3 after test
T8 Ambient temperature --
Figure 10a. View 01 of cell M4 before test Figure 10b. View 02 of cell M4 before test
Figure 10c. View of cell M4 during test_E3 Figure 10d. View of cell M4 during test_E4
T7 -- --
T8 Ambient temperature --
Thermocouple information:
Type K, 24AWG
Figure 12a. View 01 of cell M5 before test Figure 12b. View 02 of cell M5 before test
Open Location of
Surface
circuit Surface temperature
Weight Weight temperature
Sample voltage Weight temperature at measured at
before test after test at the onset
No. before loss (g) cell venting the onset of
(g) (g) of thermal
test (°C) thermal
runaway (°C)
(Vdc) runaway
Center of
M1 3.329 5570 4330 1240 125.5 167.6 cell side
face*
Center of
M2 3.347 5580 4330 1250 132.0 158.8
cell side face
Center of
M3 3.352 5610 4320 1290 106.4 174.8 cell side
face*
Center of
M4 3.337 5580 4340 1240 146.6 185.4 cell side
face*
M5 3.341 5580 4390 1190 -- -- --
Average Surface Average Surface
temperature at cell temperature at the
venting (°C) onset of thermal
runaway (°C)
127.6 171.7
Supplementary information :
1. The average surface temperature was calculated based on Cell M1, Cell M2, Cell M3 and Cell M4.
2. Remark *: Center of cell side face, near positive terminal.
Figure 14. Pressure and O2 concentration within pressure vessel before test
Table 13: Gas composition during test
Supplementary information :
The initial atmospheric component in pressure vessel was mostly N2, which makes up more than 99% by
volume before test. After test, the proportion of N2 reduced to 37.852%, due to the gas generation from cell
venting.
Figure 15. GC-TCD Spectrum and GC-FID Spectrum for gas composition gathered during test
Requested Synthesis
Gas Name Chemical Formula
Concentration (Vol%) Concentration (Vol%)
Hydrogen H2 41.920 42.013
Carbon Dioxide CO2 26.806 26.700
Carbon Monoxide CO 11.824 11.800
Methane CH4 6.813 6.820
Acetylene C2H2 0.287 0.286
Ethylene C2H4 7.916 7.880
Ethane C2H6 1.303 1.320
Propane C3H8 0.316 0.316
Propylene C3H6 1.003
1.020 (Propylene)
Cyclopropane C3H6 0.002
Propadiene C3H4 0.004
0.012 (Propyne)
Propyne C3H4 0.007
Isobutane C4H10 0.013
0.124 (Butane)
Butane C4H10 0.111
2-Methylpropene C4H8 0.056
N-Butene C4H8 0.276 0.510 (N-Butene)
2-Butene C4H8 0.161
Butylene C4H6 0.007
0.104 (1,3-Butadiene)
1,3-Butadiene C4H6 0.097
-- C5+ 0.494 0.502
-- C6+ 0.584 0.593
Supplementary information :
Remark*: Synthetically replicated gas contains no N2.
1. Copyright © 2021 SGS-CEC New Energy Technology (Chongqing) Co., Ltd. All rights reserved.
This publication may be produced in whole or in part for non-commercial purposes as long as SGS-
CEC is acknowledged as copyright owner and source of the material. SGS-CEC takes no
responsibility for and will not assume liability for damages resulting from the reader’s interpretation of
the reproduced material due to its placement and context.
2. According to the standard, instruction sheets and other texts required by the standard should be
written in the official language(s) of the country in which the product is to be sold. The applicant
should ensure that the product in future production fulfils the receptive standard requirements.
3. The components performed satisfactorily during testing and are considered to be suitable for use in
the sample tested.
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