Professional Documents
Culture Documents
TECHNICAL
SPECIFICATION
SUMMARY
2 - REFERENCES
3 - TECHNICAL REQUIREMENTS
4 - QUALIFICATION REQUIREMENTS
5 - BATCHES
6 - QUALITY CONTROL
7 - RECOMMENDED LIMITS
8 - MARKING
This specification :
- defines technical requirements, qualification and quality control conditions (product
qualification, batch control, acceptance) and test and measurement methods to be used by
manufacturers of fire-resistant phosphate-ester-base fluids used for hydraulic transmissions.
- is applicable to all new hydraulic fluids. Quality control requirements are only applicable to
manufacturers of previously qualified fluids. Test methods and associated meas urement
methods are applicable to all manufacturer's laboratories.
The content of this document is the property of AIRBUS FRANCE. It is supplied in confidence and commercial security on its contents must be
maintained. It must not be used for any purpose other than that for which it is supplied nor may information contained in it be disclosed to
unauthorized persons. It must not be reproduced in whole or in part without permission in writing from AIRBUS FRANCE.
AIRBUS FRANCE Trade Secrets or Commercial or Financial information, 5 U.S.C. (b) (4).
2 - REFERENCES
Applicable standards for the technical qualification requirements specified in section 4 are listed in
APPENDIX A1. "Equivalent" standards are listed in APPENDIX A2.
Note : the latest issue of these documents shall apply, unless specified otherwise.
3 - TECHNICAL REQUIREMENTS
The manufacturer shall guarantee the continuing availability of the hydraulic fluid.
Delivered product must be of the same quality as the qualified product and its composition
shall not be modified without AIRBUS FR prior agreement.
All delivered hydraulic fluids must be fully compatible with any other ester phosphate base
fluid already qualified, whatever the mixture proportions (Refer to APPENDIX E1).
3.2 - Types of fluids : fluids covered by this specification are listed in the table below with their
corresponding properties and in APPENDIX E1, in keeping with High Density fluid limitation
of use.
Table 1
3.3 - Physical and chemical properties : the main physical and chemical properties of the fluid
covered by this specification are listed in the Table 2 - Technical data sheet below.
3.5 - Certified laboratories : manufacturer's laboratories must be ISO certified and evaluated by
AIRBUS FR (Quality Department)
4 - QUALIFICATION REQUIREMENTS
The fluid must undergo the two qualification stages below, in the order indicated.
The manufacturer shall perform preliminary tests, as defined contractually, and submit test reports
to AIRBUS FR. These reports shall describe test results and methods applied, and indicate test
laboratories used (under GIE EADS CCR check).
AIRBUS FR reserves the right to perform all or part of preliminary tests itself, on samples of the
fluid to be qualified that the manufacturer shall supply to AIRBUS FR on request.
4.1 - Absolute kinematic viscosity "ν" of the fluid shall be determined at the temperatures
indicated below using UBBELOHDE-type viscosimetric capillary tubes in accordance with
standard ISO 3104 (ASTM D 445).
2 -1
Values, in mm .s (centiStokes) shall be :
Table 3
Temperatures Type
(°C) (°F) IV High Density (HD) IV & V Low Density (LD)
-54 -65 ν ≤ 2 900 ν ≤ 2 000
- using the electrochemical method " KARL FISCHER " in compliance with standard
ISO 12937 (ASTM D 6304),
- by turn back of a solvent mixture (4 volumes of Chloroform/1 volume of Methanol) slightly
3
hydrated with 5 mg of H2O per cm of mixture.
The water content, in % mass, shall be (all fluids) : ≤ 0.20
4.3 - Density "ρ" shall be determined at (+23 ± 3) °C in compliance with standard ISO 3675
(ASTM D 1298).
-3
Values, in kg.m , shall be : Type IV High Density HD : 990 to 1 066
Type IV & V Low Density LD : 970 to 1 020
The acidity or alkalinity of the fluid shall be determined using the colour indicator titration
method in accordance with standard NF ISO 6618 (ASTM D 974).
The acidity index values obtained, in mg KOH per gramme of fluid shall be :
Type IV : AI ≤ 0.15 and Type V : Al ≤ 0.10
All other additives not dully identified in the fluid manufacturer formulation will be
considered as contaminant and consequently prohibited, except total chlorine when its
concentration is:
TYPE IV: [Cl ] ≤ 50 p.p.m. ; TYPE V : [Cl ] ≤ 30 p.p.m.
To determine the total chlorine concentration, the hydraulic fluid shall be diluted 50/50 in
acetone. The test quantity, (25 to 50 µl according to the chlorine content), shall be injected
with a microsyringe into an oven at +1 050 °C to mineralise it by combustion in an oxygen
current. The chlorine, converted into chloride ions and conveyed by the oxygen shall
bubble into a microcell containing an electrolyte composed of isopropanol (300 ml), acetic
acid (20 ml), nitric acid (2 ml) and water (1 ml). Titration shall be by precipitation of silver
4.7 - Pour point temperature (all fluids) shall be determined in compliance with standard
NF ISO 3016 (ASTM D 97-93).
Temperature shall be :
POUR POINT : ≤ -62 °C / -80 °F
4.8 - Flash point and fire point temperatures in an open vessel (all fluids) shall be determined
using the CLEVELAND method in compliance with standard ISO 2592 (ASTM D 92-90).
Temperatures shall be :
FLASH POINT : ≥ +160 °C / +320 °F
FIRE POINT : ≥ +177 °C / +350 °F
4.9 - Auto-ignition temperature (all fluids) shall be determined in compliance with method given
hereafter.Temperature shall be :
4.9.1.2 - This standard should be used solely to measure and describe the
properties of materials, products, or systems in response to heat and
flame under controlled laboratory conditions and should not be
considered or used for the description, appraisal, or regulation of the
fire hazard materials, products, or systems under actual fire conditions.
4.9.3 - Apparatus
4.9.3.2 - Furnace
3
A 0,25 or 1 cm hypodermic syringe equipped with a 2 inches (50,8
3
mm) No. 18 stainless steel needle and calibrated in units of 0,01 cm
should be used to inject the sample into the heated test flask.
4.9.3.5 - Thermocouples
4.9.3.6 - Timer
4.9.4 - Procedure
3
Inject 0,07 cm of the sample to be tested into the test flask with the
hypodermic syringe ; quickly withdraw the syringe.
Start the timer as the sample is injected into the test flask.
4.9.4.4 - Observations
4.9.4.6 - Data : record the test temperature, pressure, quantity of sample used,
and time lag before ignition. A plot of the ignition temperature against
4.9.5 - Report
4.9.6 - Precision
4.9.6.1 - The following criteria should be used for judging the acceptability of
results (95 % confidence).
4.9.6.1.1 - Repeatability
4.9.6.1.2 - Reproducibility
Table 4
Table 5
The new fluid shall be of a purple colour which shall not significantly alter during use in
normal conditions of temperatures (-40 °C to +110 °C), or in the presence of air.
New fluid shall be clear and homogeneous without any solid suspended matter.
The colour and condition of the new fluid shall be inspected under white light shone
through a glass test tube approximately 45 mm in diameter, filled with fluid.
Note : fluid colour change can be accepted after use.
4.12 - Adiabatic Bulk Modulus (modulus of volume elasticity)
A possible method would be to determine the speed of sound "C" by measuring the time
required by an ultrasonic signal to cover a distance measured in the fluid at a required
temperature and pressure and also the density "ρ" of the fluid in the same conditions of
temperature and pressure.
In this case, the Adiabatic Bulk Modulus will be calculated in Pa by the relationship :
2
Ea = ρ x C
where
-3
ρ = density in kg.m
-1
C = speed of sound in the fluid in m.s
5
The Adiabatic Bulk Modulus, at a pressure of 210 x 10 Pa and for the temperatures range
(+25 ; +50 ; +80 ; +100 ; +120) °C, whatever the fluid type, shall be :
5
Ea ≥ 14 500 x 10 Pa
4.13 - Thermal expansion coefficient "α" (all fluids) shall be determined in compliance with the
method described in ASTM D 941 or ASTM D 1217.
-1
Value, in °C , between +25 °C and +99 °C, shall be (all fluids) :
-3
α ≤ 1 x 10
4.14 - Dielectric resistance (all fluids) shall be determined in compliance with the method
ASTM D 877.
The manufacturer shall indicate the value measured on the test fluid.
4.15 - Specific heat (all fluids) shall be determined in compliance with the method ASTM D 2766.
The manufacturer shall indicate the value measured on the test fluid.
4.16 - Solid particle contamination (Cleanliness Class determination by microscopic counting)
Note : by reason of the chemical nature of this type of hydraulic fluid, filtering membranes
compatible with phosphate esters (PA 6.6, PTFE, POM,...) with a pore dimension
of 1 µm will be used with trichlorethylene filtered at 1 µm as a solvent.
4.16.1 - Counting degree shall be determined in compliance with the method described in
NF L 41-102 (ARP 598).
3
The particles shall be counted by filtering 100 cm of fluid using a filter of the type
described above, divided into 100 equal squares, under reflected light as follows :
- For particles > 50 µm in dimension and fibres, a global count is made over the
entire surface of the filter magnified by 40.
- For particles of ∈ ] 15 ; 50 ] µm in dimension, a count is made over 10 squares
3
magnified by 100 ; this is multiplied by 10 to obtain the count for 100 cm of
fluid.
- For particles of ∈ [ 5 ; 15 ] µm in dimension, a count is made over 10 surfaces
2
of 1,5 mm magnified by 100 ; this is multiplied by 64 to obtain the count for
3
100 cm of fluid.
3
Table 6 - Number of particles per 100 cm of fluid / Class
Particle size (µm) New Fluid Before A/C delivery Aged Fluid
Value shall be :
3
≤ 1 mg for 100 cm of fluid
4.17 - Foaming (all fluids) : a foaming test shall be performed in accordance with standard
ISO 6247 (ASTM D 892) on a first test sample at +24 °C, then on a second test sample at
+93 °C and at +24 °C once the foam has disappeared.
- After bubbling the first sample for 5 minutes at +24 °C, the volume of foam shall
3
be ≤ 250 cm .
- After bubbling the second sample at +93 °C, the volume of foam shall
3 3
be ≤ 150 cm , then ≤ 450 cm after bubbling at +24 °C.
4.17.2 - Foam persistence :
- No foam must remain after allowing the first sample of fluid bubbled at +24 °C
to stand for 100 seconds.
- No foam must remain after allowing the second sample bubbled at +93 °C to
stand for 50 seconds ; no foam must remain at +24 °C after 250 seconds.
Foam volumes and persistence values must not exceed those indicated in Table
below.
Table 7
The manufacturer must specify the toxicity characteristics of the hydraulic fluid :
a) The fluid must contain no ingredient of an unknown degree of toxicity and no mixture
of ingredients liable to constitute a health hazard when the fluid is used in accordance
with instructions.
Drainage of fluid residues should entail no difficulties.
c) All studies on toxicity must be sufficiently detailed to enable easy elimination of the
toxic effects of the fluid.
If this type of study has already appeared in current publications considered as highly
qualified in this field, the articles concerned may be quoted instead of a report on the
studies themselves.
The MSDS (Material Safety Data Sheet) giving the names and quantities of chemical
products contained in the product must be provided whatever the case.
4.19.1 - Shear stability using a sonic oscillator shall be determined in compliance with the
ASTM D 2603 test method.
After testing, the absolute kinematic viscosity of the fluid shall be measured at
+38 °C as indicated in paragraph 4.1 above.
The value measured shall not vary by more than 25 % with respect to that
obtained with a new fluid, also at +38 °C.
4.19.2 - Thermal, corrosion and oxidation stability : The fluid shall be tested after
immersion of test pieces assembled in accordance with in Figure 1 below.
3
Mg
2 holes Ø 1,5
Steel
25
Al
Cadmium-plated steel
Dimensions in mm. Cu 25
Figure 1 - Arrangement of test pieces
Polished test samples : electrolytic copper (99,9 %), non-plated 2024 aluminium,
G-A3Z1 magnesium and XC18S steel.
Polished test pieces : cadmium-plated steel (7 to 12 µm plating) without chrome
finish (white).
Tests shall be performed on metal plates after immersion in the fluid. The
magnesium, aluminium, copper and steel test pieces shall be placed so that they
form a diamond, and the cadmium-plated steel test piece placed diagonally,
keeping strictly to the order indicated. The edges around the holes of the test
pieces may be touching, but the magnesium test piece must not touch the copper
piece under any circumstances in order to avoid galvanic coupling. The test piece
assembly shall be held in place by threads that are not affected by phosphate
esters (polyamide 6.6, flax fibre, etc.).
At the end of each immersion cycle indicated in paragraph 4.19.2.1 and at the
end of 4.19.2.2, in addition to the physical and chemical characteristics of the
unfiltered fluid, the metals in contact with the fluid shall be examined for
corrosion, and the fluid's oxidation resistance determined.
Metal plates shall be examined for corrosion after removing any traces of grease,
and their corrosion stability determined by measuring the variation in mass in
-2
mg.cm . No pitting, corrosion attacks or discoloration must be visible on the
surface of the metals when examined at a magnification of 20.
The acidity index per gram of fluid, measured as defined in paragraph 4.4 above,
shall be :
AI ≤ 0.5 mg KOH
4.19.2.1 - Thermal stability (all TYPE of fluid - “dry” condition i.e. [H2O] = 1000 p.p.m.
maxi)
Test equipment :
- borosilicate glass test tubes (50 ml)
- hypodermic syringe (50 ml with 90 mm needle)
- test tube rack
- pipe cleaner
- tweezers
- glass paper (600 grain)
- paper towels
- distilled water
- 4 glass pipettes with polyethylene capsules
- rubber stopper
- goggles
- indelible marker pen "ONYX"
- 250 ml glass beaker
- acetone
- iron wire, diameter 1,60 mm
- copper wire, diameter 1,60 mm
- ruler
- cotton cloth
- metal file
- 8 flasks (2 ml)
Test method :
- Obtain the required fluid water content (see paragraph 4.2)
- Fill test tubes until 85% of fluid
- Put a piece of copper wire and metalloid wire into each test tube (cut to length to fit inside
tube) and seal
- Place the test tubes in an oven pre-heated to the required constant temperature, and
remove each test tube after exposing for the required period of time
Fluid manufacturer shall draw up fluid lifetime curves showing the evolution of the hereafter
fluid intrinsic characteristics :
- γ = f, g(t,T),
- ν = f, g(t,T),
- AI = f, g(t,T),
up to reach their respective limit values as specified in hereafter Chapter 7, under the
following conditions:
- fluid temperature = from 0 °C to +200 °C
- water content = 0,20 %, 0,35 %, 0,50 %
- chlorine content : 50 p.p.m., 200 p.p.m.
4.21.1 - Compatibility between fluids (all types) : different fluid mixtures shall be placed in
glass receptacles, in proportions of 25/75, 50/50 and 75/25 % by volume, and any
visible reactions noted.
4.21.1.1 - Miscibility
After mixing the previously qualified fluids in the proportions and under
the conditions indicated above, the fluids shall be observed for colour,
turbidity, foaming, suspended particles and any other sign of
incompatibility. A change in colour is an acceptable reaction.
Tendency to foam :
- after bubbling the first sample for 5 minutes at +24 °C, the volume of
3
foam shall be ≤ 400 cm .
- after bubbling the second sample at +93 °C, the volume of foam shall
3 3
be ≤ 425 cm , then ≤ 425 cm after bubbling at +24 °C.
Foam persistence :
- no foam must remain after allowing the first sample bubbled at +24 °C
to stand for 250 seconds.
- no foam must remain after allowing the second sample bubbled at
+93 °C to stand for 200 seconds ; no foam must remain at +24 °C
after 220 seconds.
- no foam must remain at +24 °C after 220 seconds.
Foam volumes and persistence values must not exceed those indicated
in Table 9.
Table 9
The painted test pieces are polymerized for 7 days at + 20 °C and then
shall be scratched down to the metal parallel to the sides and shall be
immersed in the fluid at +70 °C for 1 000 hours.
The following initial characteristics shall be determined per grid
adherence test in accordance with ISO 2409 and, before and after
immersion cycle, hardness, under 1 200 g weight per ISO 1518, in
accordance with ISO 2812 (after leaving the test piece to cool to
+20 °C, by immersing in cool fluid).
4.21.5.1 - Adhesives
4.21.5.2 - Composites
4.23 - Second stage : Erosion test of the fluid on hydraulic test bench
The aim of the erosion test is to compare the performances of the new TYPE V fluid to be
qualified to that of the TYPE IV fluid already qualified for the same fluid manufacturer
(Erosion Reference Test), particularly regarding the electro-chemical phenomenon on the
hydraulic equipment.
4.23.1 - Test Bench definition (system representative of one aircraft hydraulic system)
The list of equipment used on the bench, along with the references, is given in
APPENDIX F1.
The diagram of the test bench is given in APPENDIX F2.
The operating principle of the bench is as follows : hydraulic power supplies a
consumer circuit comprised of three servocontrols, a braking system and a motor
unit ; an electronic box controls each item of consumer equipment, with a given
operating cycle.
The temperature of the hydraulic fluid shall be controlled by a by-passable
exchanger that must not produce copper ions.
The nominal pressure supplied by the pump is 21 MPa.
The pressure and temperature parameters are permanently monitored : any
abnormal values leads to bench shutdown.
The hydraulic reservoir is air pressurized to a relative pressure of 35 kPa, with
direct contact between the air and the hydraulic fluid.
Bench capacity is approximately 70 litres, including that of the reservoir which is
26 litres (normal filling level).
The overall internal leakage of the bench shall be measured with a flowmeter.
Individual internal leakage of consumer equipment items (1, 2, 3, 4, 5) shall be
measured using an accurate method (1 % maximum error) which shall minimize
the quantity of lost fluid.
The bench fluid cleanliness class shall be maintained at ≤ 8 (see § 4.16)
Note : this test should be performed one time with the yet qualified fluid (as
reference) and repeated with the fluid to be qualified.
d) Analysis of results
Table 11 - Analysis of the test fluid sampled during and after the test
Sleeve ≤ 25 ≤5
5 - BATCHES
A manufacturing batch is constituted with a quantity of fluid derived from a same manufacturing
cycle.
6 - QUALITY CONTROL
The manufacturer will carry out the manufacturing tests described in paragraph 6.1.1 on
each manufacturing batch.
The series of tests will be carried out on the product placed in a single recipient.
The results will be set out in an inspection document and transmitted to the buyer on
delivery with the certificate of compliance.
The manufacturer will be carried out the following tests, as described in paragraph 4, on
each batch:
- absolute kinematic viscosity (see paragraph 4.1) at -54 °C, +38 °C and +99 °C,
- density at +23 °C (see paragraph 4.3),
- pour point (see paragraph 4.7),
- flash point and fire point in an open vessel (see paragraph 4.8),
- self-ignition temperature (see paragraph 4.9),
- solid particle pollution (see paragraph 4.16),
7 - RECOMMENDED LIMITS
The hydraulic fluid criterion values below represent the permissible limits for all fluids. The In-
Service limits values (after A/C delivery below) are also specified in the Aircraft Maintenance
Manual.
8 - MARKING
. On recipients :
- the manufacturing batch number,
- the fill-up date.
The fluid will be delivered in air-tight containers which be stored in a dry place.
A2 Equivalent standards 2 31
Document Title §
AIR 1651 Lubricating oil test (laboratory test) 4.19.2.2
ASTM D 2603 ASTM for sonic shear stability of polymer-containing oils 4.19.1
ASTM D 2266 ASTM for wear preventive characteristics of lubricating grease (4 - balls) 4.22
ASTM for electrical dielectric break -down voltage of insulating liquids using
ASTM D 877 4.14
disk electrodes
prEN2243-2 Metal-metal peel test using Bell floating-roller test method 4.21.5.1
EN 2591-315 Elements of electrical and optical connection Test methods Fluid resistance 4.21.5
EN3475-411 Cables, electrical, aircraft use Test methods Fluid resistance 4.21.5
NFL 41-102 Pollution of hydraulic circuits by solid particles - Test method 4.16
ISO 2409 +
Paints - Grid tests on varnish and paints on a metal support 4.21.3
ISO 1518 & 2812
ISO 3675 Petroleum products - Density of petroleum products - Areometer method 4.3
ISO 2592 Petroleum products - Flash point and fire point in an open receptacle 4.8
Document Title §
ARP / AS 598 Aerospace microscopic sizing and counting of particulate contamination for
4.16.1
OR ASTM F 661 fluid power systems
ASTM D 1298 Standard test method for density and relative density (specific gravity) 4.13
ASTM D 445 Standard test method for determination of the absolute kinematic viscosity 4.1
ASTM D 892 Standard test method for foaming characteristics of lubricating oils 4.17
ASTM D 92 Standard test method for flash and fire points by Cleveland open cup 4.8
ASTM D 974 Standard test method for acid and base number by colour indicator titration 4.4
Note : this above list is only indicative. In case of dispute, only the standards referenced in above
APPENDIX A1 will be considered.
Dimensions in mm.
0 250 44 8 2 0
C 1 500 89 16 3 1
L 2 1 000 178 32 6 1
3 2 000 356 63 11 2
(*)Including fibres: a fibre is a particle with a length over 100 µm and a ratio length /width of 10
Dry Manometer
Air or Nitrogen
Source
Shut-off Valve
(SOV)
Self-Regulating
Pressure
Reducing Valve Pressurised
Container
Membrane Fitting
Graduated Flask
1-Store the fluid sampling at ambient temperature condition in hermetic flask during 24 hours in respect. Rinse correctly all
components (membrane + support) with filtered cleaning liquid through a DPM membrane (filterability less than 0,8 µm), dry
with filtered and pressurised air, the apparatus being maintained in a position facilitating the running of cleaning liquid. The
filtering membranes have to be dried in drying-oven at between 60 to 80°C temperature during minimum 10 minutes.
2-Install the components, with electrical bonding for m etallic parts, and put the filtering membrane on the support screen
using a nipper.
3-Shut the SOV and set the air or gas pressure at (1 ± 0,05) bar.
4-Pour around 320 cc of homogenised and de-aerated fluid to be tested on the pressurised container and shut hermetically it.
5-Open the SOV to pressurise the container.
Note: 4 and 5 will be quickly operated
6-The chronometer has to be triggered, monitoring a constant pressure (see 3) when the first drop of fluid is falling in the
graduated flask.
7-Record the corresponding time for each required volume (t50 for 50 cc, t100 for 100cc, t200 for 200cc, t 300 for 300cc) in a
sheet of results (table presentation recommended) giving the associated installation and room conditions and, if known, the
fluid cleanliness class (as per NS307110 § 4.16) and the fluid contamination (water and chlorine concentrations for aged
fluid) .
Notes:
1: if the measured time t50 were < 60 seconds, the test would be stopped and performed again with a pressure of (0,5 ± 0,05)
bar.
2: if the measured time t50 were < 600 seconds, the test would be stopped and performed again with a pressure of (2, 0±
0,05) bar.
3: stop the test after 2 hours (7200s) and record the total volume of filtered fluid.
4: perform each test 3 times for each referenced volume.
8-Shut the SOV and remove the components.
9-Examine visually the membrane to check if its colouring is homogeneous. If it is not the case, please, note that in the test
report.
10-Clean the components and rinse the pipes of testing installation using appropriated cleanliness liquid.
SKYDROL 500B-4
Not to be used
High
on Airbus serial production lines.
(*)
IV Forbidden
for new Airbus programs (*)
PLUS
Low HyJet IV-A SKYDROL LD-4
V Low HyJet V
(*) Please, consult the list of authorized fluid given in respective CML and AMM for each Airbus
aircraft.
Tensile strength
Composite
σr, MPa σr / +23 °C ≥ 16
adhesive
REDUX 322
Peel : Flux, N.m/m at +23 °C ≥ 5
Tensile strength
Composite
σr, MPa σr / +23 °C ≥ 33
adhesive
AF 3109-2K
Peel : Flux, N.m/m at +23 °C ≥ 60
Interlaminar shear
τ, MPa τ / +23 °C ≥ 90
Failure type "in shear"
Composite
T300 Pure bending
BSL914-34 % Modulus of elasticity
E, GPa E ≥ 105
Interlaminar shear
τ, MPa τ / +23 °C ≥ 50
Failure type "in shear"
Composite
Pure bending
V913-54 %
Modulus of elasticity
G973
E, GPa E ≥ 28
3
800 cm capacity 60
7 20
Pressure (bar)
BRAKING BLOCK 4
1
6 bars
49 50
Time (seconds)
Blanked reservoir return
Return pressure =
3
supply pressure = 155 bars
45 46
1
Operating pressure
SUPPLY PRESSURE
SERVOVALVE CURRENT
Supply pressure
10 brakes 30 sec.
Return pressure = Reservoir pressure = 6 bars
3
1
15
9 ±1,7 mA - 10 Hz sinus
10 sec.
5
4 sec.
bars
4
0
6
18
206
150
80
36
Current (mA)
B.04.77
C.04.79
D.01.80
NOTE : Modification to the last standard issue are indicated by a vertical line
in the margin.
NOTE : Modification to the last standard issue are indicated by a vertical line
in the margin.
NOTE : Modification to the last standard issue are indicated by a vertical line
in the margin.
NOTE : Modification to the last standard issue are indicated by a vertical line
in the margin.