IPC-TM-650 EN 2022 试验方法.pdf - 第189页
5.2.4 After 16 hours ± one hour, remove the bags from the water bath and shake vigorously for 10 seconds to mix the contents. 5.2.5 Allow the solutions to cool for 30 minutes minimum before transferring the extract solut…

1
Scope
This
test procedure is designed to measure the
level of chloride, bromide, and fluoride present in a soldering
flux or paste by Ion Chromatography.
2 Applicable Documents
IPC J-STD-004
Requirements
for Soldering Fluxes
IPC-TM-650
Test
Methods Manual
2.3.34 Solids Content, Flux
3
Test Specimens
3.1
Liquid
flux, solder paste, paste flux, extracted solder
preform flux, or cored wire. The reflow/extraction process
should be carried out in accordance with J-STD-004 for the
solder preforms.
4
Apparatus and Material
4.1
Ion
Chromatograph capable of 50 ppb or better detec-
tion. The equipment and chemistry should be set up and stan-
dardized per the manufacturer’s instructions.
4.2
Hot
Water Bath capable of maintaining 80 ± 5 °C [176 ±
9 °F].
4.3
Clean,
heat sealable bags, i.e., KAPAK® 500 series or
equivalent, with less than 250 ppb extractable contaminants.
(Specify cleanliness level or manufacturers’ part number.)
4.4
Cleanroom
vinyl gloves. (<3 ppm of Cl).
4.5
Deionized
water with a resistivity of at least 18.0
megohm centimeter.
4.6
HPLC
or ASC grade chemicals for eluent and regener-
ant preparation.
4.7
NIST
traceable standards for chloride, bromide and fluo-
ride.
4.8
2-Propanol
(IPA), Electronic grade or better.
4.9
Solder
Pot.
4.10
Analytical
Balance capable of measuring 0.001g.
4.11
50
mm [1.969 in] mandrel.
4.12
Clean
wire cutters.
4.13
Heat
sealer.
4.14
Ion-free
containers.
4.15
Ultrasonic
bath or magnetic stirrer and stir bar.
4.16
Ion-free
syringe filters.
4.17
Test
Tube.
5
Procedures
5.1 Liquid Flux / Extracted Flux
5.1.1
Prepare
a solution of 10% by volume isopropyl alcohol
and 90% by volume deionized water and dilute the liquid flux
sample to 200X.
5.1.2
Filter
samples through ion-free syringe filters to
remove particulate prior to analysis.
5.2
Solder Paste/Paste Flux
5.2.1
Weigh
to the nearest 0.001 g., approximately one (1)
gram of solder paste and place it into a tared 165 mm
[6.496 in] by 200 mm [7.874 in] Kapak® bag containing 50 ml
of a solution of 10% by volume isopropyl alcohol and 90% by
volume deionized water.
5.2.2 Prepare
a blank by adding 50 ml of the extract solu-
tion to an empty bag.
5.2.3
Label
and heat seal the bags and place them into a
hot water bath maintained at 80 °C [176 °F].
2215
Sanders Road
Northbrook, IL 60062-6135
IPC-TM-650
TEST
METHODS MANUAL
Number
2.3.28.1
Subject
Halide
Content of Soldering Fluxes and Pastes
Date
06/04
Revision
Originating Task Group
Flux Specifications Task Group (5-24a)
Material
in this Test Methods Manual was voluntarily established by Technical Committees of IPC. This material is advisory only
and its use or adaptation is entirely voluntary. IPC disclaims all liability of any kind as to the use, application, or adaptation of this
material. Users are also wholly responsible for protecting themselves against all claims or liabilities for patent infringement.
Equipment referenced is for the convenience of the user and does not imply endorsement by IPC.
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5.2.4
After
16 hours ± one hour, remove the bags from the
water bath and shake vigorously for 10 seconds to mix the
contents.
5.2.5
Allow
the solutions to cool for 30 minutes minimum
before transferring the extract solutions to ion-free plastic con-
tainers.
5.2.6
Filter
samples through ion-free syringe filters to
remove particulate prior to analysis.
5.3
Flux-Cored Solder Wire
5.3.1
Weigh
approximately fifty (50) grams of the wire
sample.
5.3.2 Wrap
the specimen around a 50 mm [1.969 in] diam-
eter mandrel (Note: Touch the cut ends of the sample with a
soldering iron to seal the sample while cleaning). Place the
resultant sample coil into a beaker of boiling deionized water.
5.3.3
After
approximately five (5) minutes, remove the coil
from the boiling water, rinse with isopropyl alcohol, and allow
to air dry.
5.3.4
After
drying, cut the sample into approximately one (1)
centimeter [0.394 in] length pieces and place inside of a test
tube.
5.3.5
Place
the test tube, with diced sample, in a solder
bath. Thirty (30) seconds after the sample is completely
reflowed, remove the test tube and then allow the solder to
solidify.
5.3.6
Upon
solidification of the solder and before solidifica-
tion of the flux, pour approximately 0.2 grams of the flux into
a test tube of known weight.
5.3.7
Weigh
the second test tube containing the flux and
subtract off the test tube weight to determine the weight of
the flux sample.
5.3.8
Add
a known volume of isopropyl alcohol to the
sample test tube and place the test tube into a sonicator or on
a magnetic stirrer with a stir bar in the test tube for approxi-
mately thirty (30) minutes.
5.3.9
Once
the flux sample is dissolved, dilute the sample
solution such that the overall concentration of isopropyl alco-
hol is approximately 10%.
5.4
Test Method
5.4.1
Extract
solutions shall be analyzed using an Ion Chro-
matograph with a three to five level calibration.
5.4.2
Dilute
extract solutions further with a 10% by volume
isopropyl alcohol solution, if necessary, to lower ion concen-
tration levels within the calibration ranges of the chromato-
graph.
5.5
Calculations
5.5.1 Liquid Flux
5.5.1.1
Determine
the weight of each halide ion in the liquid
flux:
Weight of halide ion (g) in liquid flux =
[ppm from IC (µg/mL)] x
[Dilution factor, if necessary] x
[Volume of dilution solution (ml)] x 10
-6
Note: ‘‘ppm
from IC’’ value is actually specimen value minus
blank value.
5.5.1.2
Determine
the weight of flux solids in the liquid flux:
Weight of flux solids (g) in liquid flux =
[Volume of liquid flux sample (ml)] x
[Density of liquid flux sample (g/ml)] x
[% Solids in liquid flux / 100]
5.5.1.3
Calculate
percent of each halide ion in the nonvola-
tile solid portion of the liquid flux:
Percent of halide ion in solid portion of liquid flux =
[Weight of halide ion (g) in liquid flux] x 100
[Weight
of flux solids (g) in liquid flux]
5.5.2
Solder Paste
5.5.2.1
Determine
the weight of each halide ion in the sol-
der paste flux:
Weight of halide ion (g) in solder paste flux =
[ppm from IC (µg/mL)] x
[Dilution factor, if necessary] x
[Volume of extract solution (mL)] x 10
-6
IPC-TM-650
Number
2.3.28.1
Subject
Halide
Content of Soldering Fluxes and Pastes
Date
06/04
Revision
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5.5.2.2
Determine
the weight of flux solids in the solder
paste flux:
Weight of flux solids (g) in solder paste flux =
[Weight of solder paste sample (g)] x
[% Flux in solder paste / 100] x
[% Solids in paste flux / 100]
5.5.2.3 Calculate
the percentage of each halide ion in the
nonvolatile solid portion of the liquid flux:
Percent of halide ion in solid portion of solder paste flux =
[Weight of halide ion (g) in solder paste] x 100
[Weight
of flux solids (g) in solder paste]
5.5.3
Flux-Cored Solder Wire
5.5.3.1
Determine
the weight of each halide ion in the sol-
der wire flux:
Weight of halide ion (g) in solder wire flux =
[ppm from IC (µg/mL)] x
[Dilution factor, if necessary] x
[Volume of dilution solution (ml)] x 10
-6
5.5.3.2
Determine
the weight of flux solids in the solder wire
flux:
Weight of flux solids (g) in solder wire flux =
[Weight of flux sample (g)] x [% Solids in flux / 100]
5.5.3.3 Calculate percent of each halide ion in the nonvola-
tile solid portion of the solder wire flux:
Percent of halide ion in solid portion of solder wire flux =
[Weight of halide ion (g) in flux] x 100
[Weight
of flux solids (g) in flux]
6
Notes
6.1
When
establishing an ion chromatography method, the
containers utilized for extraction and sample processing
should be evaluated to confirm that error is not introduced by
the chosen ‘‘ion-free’’ containers.
6.2
Safety
Observe
all appropriate precautions on MSDS
for chemicals involved in this test method.
IPC-TM-650
Number
2.3.28.1
Subject
Halide
Content of Soldering Fluxes and Pastes
Date
06/04
Revision
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