ASTM B254 92 2020 E1
ASTM B254 92 2020 E1
ASTM B254 92 2020 E1
for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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4.1 The preparation of stainless steel for electroplating
This practice is under the jurisdiction of ASTM Committee B08 on Metallic
and Inorganic Coatings and is the direct responsibility of Subcommittee B08.02 on
involves three basic steps in the following order:
Pre Treatment. 4.1.1 Removal of scale. If scale removal is necessary, one of
Current edition approved Nov. 1, 2020. Published December 2020. Originally the methods outlined in Appendix X2 may be used (Note 1).
approved in 1951. Last previous edition approved in 2014 as B254 – 92(2014). DOI:
10.1520/B0254-92R20E01. See also Practice A380.
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For referenced ASTM standards, visit the ASTM website, www.astm.org, or 4.1.2 Removal of oil, grease, or other foreign material by
contact ASTM Customer Service at [email protected]. For Annual Book of ASTM
Standards volume information, refer to the standard’s Document Summary page on
cleaning, and
the ASTM website. 4.1.3 Activation immediately before electroplating.
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B254 − 92 (2020)´1
4.2 Precleaning—Removal of fabricating lubricants and NOTE 5—The etching practice may be more severe for nondecorative
finishing compounds from the stainless steel may have to be applications than for decorative applications.
undertaken immediately following the fabrication or finishing 7.2 The following activating procedures have been used.
operation (Note 2). The procedure selected will depend upon the nature of the part
4.3 Electrocleaning—Anodic cleaning is generally preferred and preceding or subsequent processes (see 7.7). In the
(Note 3). following solution formulas, the concentrations are expressed
on a volume basis as follows:
4.4 Metal Lubricants—Metal lubricants such as copper, Liquids: as volume per litre of solution
lead, or cadmium, applied to stainless steel wire for cold Solids: as mass per litre of solution
heading, wire drawing, or spring forming are removed by
immersion in a solution of 200 mL of concentrated, 67 mass %, 7.3 The commercial grade acids and salts used in the
nitric acid (density 1.40 g/mL) diluted to 1 L at 50 to 60 °C. formulas include:
See Practice A380. Sulfuric acid: 93 mass %; density 1.83 g/mL
Hydrochloric acid: 31 mass %; density 1.16 g/mL
NOTE 1—Oil, grease or other fabricating lubricants should be removed
by cleaning before heat treating. Nickel chloride: NiCl2·6H2O
NOTE 2—Spray cleaning with a nozzle pressure of 200 to 400 kPa (30 Copper sulfate: CuSO4·5H2O
to 60 psi) in a power washer, using an alkaline or emulsion-type cleaner, Warning—Sulfuric acid should be slowly added to the
is the generally preferred method, especially for the removal of heavy approximate amount of water required with rapid mixing, and
drawing, buffing, or polishing compounds. Soak cleaning or vapor
degreasing may also be used. Extreme examples of such compounds are then after cooling, diluted to exact volume.
drawing or stamping lubricants containing unsaturated oils, which if left 7.4 Cathodic Treatments:
on the surface, form by air-oxidation tenacious films that are very difficult
to remove. 7.4.1 Sulfuric acid 50 to 500 mL/L
NOTE 3—When brightness is important, alkalinity, current density, and Water to 1 L
Temperature room
temperature should be kept as low as the part will permit. This is an
Time 1 to 5 min
essential requirement when cleaning work on racks bearing auxiliary lead Current density 0.54 A/dm2
anodes or when high chromium alloys (such as UNS Types S44200 and Anodes pure lead
S44600) are being cleaned.
5. Cleaning Solutions
iTeh Standards 7.4.2 A Hydrochloric acid
Water
Temperature
50 to 500 mL/L
to 1 L
room
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7.6 Simultaneous Activation-Electroplating Treatments: activating procedure; otherwise the surface will passivate itself
7.6.1 Nickel chlorideA 240 g and the electrodeposit will not be adherent.
Hydrochloric acid 85 mL 8.1.1 The rinse water should be kept slightly acid (approxi-
Iron should not exceed
7.5 g/L
mately pH of 2.5 to 3.5). The acid carryover from the activation
Water to 1 L operation will maintain this pH in many instances.
Temperature room 8.1.2 In conveyorized operations where trace contamination
Electrodes nickel
A
See U. S. Patent No. 2,285,548-9.
of plating solutions with chloride and sulfate from activating
7.6.1.1 Anodic Treatment:
solutions will produce an unsatisfactory electrodeposit, spray-
rinse operations subsequent to the activation treatment will
Current density 2.2 A/dm2 remove these contaminants.
Time 2 min
8.1.3 If the simultaneous activation-plating procedure is
7.6.1.2 Followed by Cathodic Treatment:
employed and nickel plating follows, the intermediate rinse
Current density 2.2 A/dm2 need only be superficial and the length of transfer time is not
Time 6 min so important.
7.6.2 Nickel chlorideA 240 g
Hydrochloric acid 126 mL 9. Electroplating
Water to 1 L
Electrodes nickel
9.1 An adherent electrodeposit of commonly electroplated
TemperatureB room metals (cadmium, copper, brass, chromium, gold, nickel, or
Current density (cathodic) 5.4 to 21.5 A/dm2 silver) may be electrodeposited directly on stainless steel
Time 2 to 4 min
A
See U. S. Patent No. 2,437,409. provided the surface of the stainless steel is active.
B
Bath may require cooling or reduction in hydrochloric acid content if
temperature exceeds 30 °C.
NOTE 8—Nickel may be electrodeposited at normal current densities
directly on properly activated stainless steel from standard nickel-
7.6.3 Nickel chloride 30 to 300 g/L electroplating solutions if the pH of the solution is between 2 and 4. A pH
Hydrochloric acid 15 to 160 mL/L
of 2 is preferred.
Water to 1 L
Electrodes nickel
NOTE 9—When a chromium-electroplating solution containing 400 g/L
iTeh Standards
Temperature room of chromic acid is used for decorative chromium electroplating, better
Current density 0.55 to 10.75 A/dm2 coverage and a wider bright range is obtained by operating at a current
Time 1⁄2 to 5 min density of 16.2 A/dm2 and 49 °C.
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7.6.4 Hydrochloric acid undiluted commercial grade NOTE 10—A bright nickel electroplate under chromium, preceded by
(7.2) one of the simultaneous activation-electroplating treatments, may often be
Copper sulfate 0.4 g/L used to advantage for better color matching and elimination of chromium
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Electrodes nickel buffing.
Temperature room
Current density 9.2 Where practical, the parts should have the current
4.5 to 6.6 A/dm2
Time 1 to 5 min applied during entry into the electroplating solution.
NOTE 7—Nickel anode materials containing greater than 0.01 % sulfur
are not recommended for use in acid nickel strike baths ASTM
operated atB254-92(2020)e1
pH 0.5,
10. Stripping
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or lower, to avoid
7.6.1-7.6.4, and 7.7).
oxidation of sulfides by hydrochloric acid (see 10.1 Nitric acid is the preferred stripping solution.
10.2 Decorative chromium electrodeposits have been
7.7 A combination of more than one type of treatment may stripped in a solution of 500 mL of concentrated, 31 mass %
be necessary to ensure a high degree of adhesion. For example, hydrochloric acid (density 1.16 g/mL) diluted to 1 L at 45 to
the following has been used in the automotive industry for 50 °C for 1 min.
nickel plating on UNS Type S30200 stainless steel:
NOTE 11—Overstripping will result in etching.
Sulfuric acid 650 mL
Water to 1 L
NOTE 12—Decorative chromium electrodeposits may also be stripped
Potential (cathodic) 10 V anodically in any alkaline solution.
Electrodes lead 10.3 Cadmium is stripped successfully without current by
Temperature room
Time 2 min immersion in a solution of 120 g/L of ammonium nitrate.
Followed by: 11. Post Electroplating Operations
Nickel chloride 240 g 11.1 Post electroplating operations such as stress relieving,
Hydrochloric acid 120 mL
Water to 1 L buffing or coloring, and forming or drawing may be applied to
Electrodes nickel stainless steel in the same manner as to any other basis metal,
Temperature room as long as the natural differences in the characteristic of the
Time 2 min
Current density (cathodic) 16.2 A/dm2 stainless steel are taken into consideration. The stainless steel
This is followed by transfer without rinsing to a Watts (or supplier should be consulted for guidance in regard to these
higher chloride) nickel bath with a pH of 1.5 to 2.0. characteristics.
12. Test Methods
8. Rinsing 12.1 The methods of testing for thickness, hardness, and
8.1 The parts should be transferred to the cold-water rinse adhesion of electrodeposits applied with the usual basis metals
and to the plating solution as rapidly as practicable after the may be employed for similar tests on stainless steel.
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B254 − 92 (2020)´1
NOTE 13—An exception to this is the determination of the thickness of penetrated, the accuracy of this method may be questionable for this
chromium on stainless steel by the hydrochloric acid drop method. application.
Because gassing continues after the chromium coating has been
APPENDIXES
(Nonmandatory Information)
X1.1 There are many standard grades and many more S30200, S30300, S30400, S30500, S30800, S30900, S31000,
special grades of stainless steel. Each grade has a specific use, S31600, S31700, S32100, and S34700 are the more common
and each may present an individual finishing problem. The alloys of this type.
common grades are classified as:
X1.1.4 Precipitation-hardening or hardenable chromium
X1.1.1 Martensitic, or hardenable magnetic chromium nickel-alloys. UNS Types S17400, S17700, S15700, and
grades. UNS Types S40300, S40500, S40600, S41000, S35000, are some examples of this type (Note X1.1).
S41400, S41600, S42000, S43100, S44002, S44003, and
S44004 are the more common alloys of this grade. NOTE X1.1—The precipitation-hardening types of stainless steel should
X1.1.2 Ferritic, or nonhardenable magnetic chromium be electroplatable by one or more of the procedures in this practice, but
difficulties may be encountered with types containing relatively high
grades. UNS Types S43000, S43020, and S44600 are alloys of levels of manganese, molybdenum, and silicon. In the fully aged
this type. condition, these grades of stainless steel may be susceptible to hydrogen
X1.1.3 Austenitic, or nonhardenable, nonmagnetic embrittlement due to electroplating (see X3.3).
chromium-nickel alloys. UNS Types S20100, S20200, S30100,
iTeh Standards
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X2. MILL FINISHES
X3.1 All of the common grades of stainless steel with finished product. Grinding checks, glazing, and heat-treating
normal heat treatments, in the full range of hardness, and in the stains on the stainless steel should be avoided.
forms mentioned above, with any surface finish free of scale,
and when properly activated may be covered with electrode- X3.3 The high-carbon grades (UNS Types 42000, 44002,
posits of commonly electrodeposited metals. 44003, and 44004) may be subject to hydrogen embrittlement
during electroplating operations. This may be overcome by
X3.2 The smoothness of stainless steel surface to be elec- heating the electroplated articles at 150 to 260 °C for 1 to 3 h
troplated should be comparable with the requirement of the after electroplating.