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SEMI G75-0698 © SE MI 1998 3 NOTICE: T hese standards do n ot purport to address safety issues, if any, ass o ciated with their use. It is the responsibility of t he user of these standards to establish appropriate safet…

SEMI G75-0698 © SEMI 1998 2
4.10 tensile break strength — The tensile force per
unit of original cross section of the sample at the point
of breakage.
4.11 tensile modulus — The ratio of stress to strain of
the sample below the yield point, in the elastic region of
the stress/strain curve.
NOTE: Plastic materials may not have a true elastic region in
the stress/strain curve or force/elongation curve. A tangent is
drawn to the maximum slope of the curve in order to
determine the modulus.
4.12 thermal decomposition temperature (base film
and adhesive) — The thermal decomposition
temperature is determined at 5% of the weight loss
when the tape is set to the thermal ramp at 10°
C/minute.
4.13 volume resistivity — The quotient of the voltage
gradient parallel to the current within the test piece
divided by the current density.
5 Significance
5.1 Ionic Impurities
5.1.1 Ionic contamination can adver sely affect the
reliability of semiconductor devices by causing leakage
currents and aluminum corrosion.
5.2 Adhesive Strength
5.2.1 Low adhesive strength may re sult in inner leads
movement of leadframe during the assembly and
packaging process which may result in low yield or
poor device reliability.
5.3 Peel Strength of Protective Film from Leadframe
Tape
5.3.1 If the peeling strength of prote ctive film from
leadframe tape varies in peeling strength, the taping
machines will not operate consistently.
5.4 Water Absorption
5.4.1 If the leadframe tapes absorb a n excessive
amount of water in storage, before or after packaging,
then reliability of devices made by these leadframes
may be affected. Current leakage and corrosion of
device metallization may occur.
5.5 Weight Loss
5.5.1 Weight loss may indicate that devices
manufactured with the leadframe tape may have
reliability problems due to the tape outgassing.
5.6 Shrinkage Factor
5.6.1 Excessive shrinkage at therma l processing may
cause the lead shift and wire bond problems for
automatic bonders.
5.7 Thermal Decomposition Temperature
5.7.1 The devices manufactured with leadframe tape
that decomposes at too low a temperature may have
lower reliability.
5.8 Coefficient of Thermal Expansion and Glass
Transition Temperature
5.8.1 Excessive expansion of the leadframe tape may
cause lead shift and/or lead lift and result in dislocated
bonds from automatic bonders.
5.9 Tensile Strength, Elongation, and Tensile Modulus
5.9.1 If the tensile strength, elongation, and tensile
modulus varies, the taping machines will not operate
consistently.
5.10 Volume and Surface Resistivity
5.10.1 Low volume and/or surface re sistivity is
indicative of potential leakage currents between
leadframe inner leads which can affect the function of
the device.
5.11 Dielectric Constant and Dissipation Factor
5.11.1 High dielectric constant mater ials used in
semiconductor packages may cause transmission
delays. High dielectric loss causes energy loss, which
leads to exothermic problems in semiconductor
packages.
5.12 Breakdown Strength
5.12.1 Very low breakdown strength may cause de-
vices to fail in use.
5.13 Leakage Current
5.13.1 A high leakage current betwee n leadframe
inner leads, which may be exacerbated due to high
moisture test conditions and impurities in the tape, may
result in poor device reliability.
6 Procedure
6.1 Procedures are detailed in the Test Methods
following this document.
7 Reporting Results
7.1 The sample size per lot and the reported items
shall be determined by agreement between user and
supplier.
7.2 The report shall contain the fo llowing information:
7.2.1 Leadframe Tape Material — M anufacturer, type,
and lot number.
7.2.2 Notification of acceptance or rejection.

SEMI G75-0698 © SEMI 19983
NOTICE: These standards do not purport to address
safety issues, if any, associated with their use. It is the
responsibility of the user of these standards to establish
appropriate safety and health practices and determine
the applicability of regulatory limitations prior to use.
SEMI makes no warranties or representations as to the
suitability of the standards set forth herein for any
particular application. The determination of the
suitability of the standard is solely the responsibility of
the user. Users are cautioned to refer to manufacturer’s
instructions, product labels, product data sheets, and
other relevant literature respecting any materials
mentioned herein. These standards are subject to
change without notice.
The user’ attention is called to the possibility that
compliance with this standard may require use of
copyrighted material or of an invention covered by
patent rights. By publication of this standard, SEMI
takes no position respecting the validity of any patent
rights or copyrights asserted in connection with any
item mentioned in this standard. Users of this standard
are expressly advised that determination of any such
patent rights or copyrights, and the risk of infringement
of such rights, are entirely their own responsibility.
Copyright by SEMI® (Semiconductor Equipment and Materials
International), 3081 Zanker Road, San Jose, CA 95134. Reproduction o
f
the contents in whole or in part is forbidden without express written
consent of SEMI.

SEMI G75.1-0698 © SEMI 19981
SEMI G75.1-0698
TEST METHOD FOR MEASUREMENT OF IONIC IMPURITIES IN
LEADFRAME TAPE
1 Summary of Method
1.1 Ionic impurities are extracted from sample tape by
water at 100°C or 121°C and quantitatively analyzed by
ion chromatography and flame photometry or atomic
absorption spectrometry. The pH and electrical
conductivity of the extracted solutions are also
measured.
1.2 If sample tape needs the cure before the extraction,
vender should inform the customer of the necessity of
curing and report the impurity data after cure.
1.3 Ion chromatography is used to determine the
presence and concentration of the following ionic
species: Na
+
, NH4
+
, K
+
, NO
3
-
, Cl
-
, Br
-
, SO
4
2-
, PO
4
3-
.
1.4 Flame photometry or atomic absorption
spectrometry is used to determine the concentration of
Na
+
and K
+
ions.
1.5 pH and conductivity measurements are also de-
scribed.
2 Referenced Documents
NOTE: As listed or revised, all documents cited shall be the
latest publications of adopted standards.
2.1 SEMI Standards
SEMI G29 — Test Method for Trace Contaminants in
Molding Compounds
SEMI G59 — Test Method for Measurement of Ionic
Contamination on Leadframe Interleafing and the
Contamination Transferred from the Interleafing to the
Leadframes
2.2 ASTM Standards
1
ASTM D 1125 — Standard Test Methods for Electrical
Conductivity and Resistivity of Water
ASTM D 1193 — Standard Specification for Reagent
Water
ASTM D 4327 — Standard Test Method for Anions in
Water by Ion Chromatography
ASTM E 70 — Standard Test Method for pH of
Aqueous Solutions with the Glass Electrode
2.3 JIS Specifications
2
1 American Society for Testing Materials, 100 Barr Harbor Drive,
West Conshohoken, PA 19428-2959
JIS K 0121 — General Rules for Atomic Absorption
Spectrochemical Analyses
JIS Z 8802 — Method for Determination of pH of
Aqueous Solutions
3 Interferences
3.1 All the sample preparations and measurements
must be carried out in clean containers which have been
washed in deionized water in order to reduce any
spurious readings.
3.2 Electrodes and syringes must be similarly cleaned
before each test.
3.3 Contamination from the sampling process may
also affect the results.
4 Equipment
4.1 Ion Extraction Vessels-Parr bomb with Teflon
liner.
4.2 Ion chromatograph for anion and cation analysis
(see SEMI G59).
4.3 Flame photometer or atomic absorption
spectrometer.
4.4 Standard solution preparation vessels, balance and
volumetric dispensers (see SEMI G29 and SEMI G59).
4.5 pH meter.
4.6 Microconductivity cell and meter.
5 Reagents and Materials
5.1 Deionized water, conductivity of less than 1.0 µ
S/cm at 25°C per ASTM D 1193.
5.2 Eluents and regenerants for specific
chromatograph columns prepared per chromatograph
equipment manufacturer’s recommendations so that the
water peak can be separated from the ionic peaks.
5.3 Compounds for Standard Solutions
5.3.1 Cations — NaCl, NH
4
Cl, KCl
5.3.2 Anions — NaCl, Na2HPO
4
•12H2O, NaBr,
NaNO
3
, K
2
SO
4
NOTE: All compounds to be reagent grade.
2 Japanese Standards Association, 1-24, Akasaka 4 Chome, Minato-
ku, Tokyo, Japan