Any
introductory course starts out with a brief history of the subject,
and this article will be no different. According to a technical
report of the International Nickel Co., Ltd., Joseph Shore applied
for a patent for nickel plating in 1840; however, it was not until
1842, in Frankfort, Germany, that Böttger succeeded in depositing
nickel from a solution of nickel ammonium sulfate.1
One
of the first United States patents was granted to Adams in 1869
for a solution of nickel ammonium chloride, and in 1878 Weston
obtained a patent for the addition of boric acid to nickel plating
solutions. Several patents were granted for various bath improvements,
until O.P. Watts developed a rapid nickel plating bath in 1916.
This nickel plating bath is still predominantly used throughout
the world and was the first to make it possible to exceed current
densities of 5 asf by a factor of 10.
Nickel
plating solutions based on sulfamate solutions were introduced
by Cambi and Piontelli in a report for the Lombard Institute of
Sciences.
Types
of Nickel Plating Solutions
Sulfate
Solutions. The
most common nickel plating bath is the sulfate bath known as the
Watts bath. Typical composition and operating conditions are shown
in Table I. The large amount of nickel sulfate provides the necessary
concentration of nickel ions. Nickel chloride improves anode corrosion
and increases conductivity. Boric acid is used as a weak buffer
to maintain pH.
The
Watts bath has four major advantages: 1) Simple and easy to use;
2) Easily available in high purity grades and relatively inexpensive;
3) Less aggressive to plant equipment than nickel chloride solutions;
and 4) Deposits plated from these solutions are less brittle and
show lower internal stress than those plated from nickel chloride
electrolytes.
High
Chloride Solutions. Chloride baths have an advantage over
sulfate baths in deposition speed; not necessarily in current
density, but in improved current distribution.
All-Chloride
Solutions. The advantages of all-chloride nickel plating solutions
include the following: 1) Low voltage; 2) Good polishing characteristics;
3) Heavy coatings can be deposited; 4) Low pitting; 5) Improved
cathode efficiency; and 6) No need to cool the plating solution.
See Table I for composition and operating parameters.
However,
there are disadvantages to this bath as well: 1) Highly corrosive;
2) Nickel chloride is sometimes less pure than nickel sulfate
(particularly important in bright nickel plating); 3) Mechanical
properties of the deposit are not as good as those from the Watts
bath.
Fluoborate
Solutions. In nickel fluorborate baths, the electrolyte is
maintained at a pH of 2.0-3.5 using fluoroboric acid. Metal content
is maintained at up to 120 g/liter of nickel, which is much higher
than in a Watt's bath. Because of this, higher current densities
are necessary.
Nickel
coatings deposited from this type of bath have properties similar
to those deposited from Watt's baths; however, these coatings
are usually specified for heavy nickel applications and electroforming.
Anode
dissolution in a nickel fluoborate bath not containing chloride
is better than in a nickel sulfate solution with nickel chloride.
Disadvantages
of fluoborate baths include the following: 1) High cost of chemicals;
2) Throwing power less than that of sulfate solutions.
Sulfamate
Solutions. This bath is based on the nickel salt of sulfamic
acid, and the pH is adjusted using sulfamic acid, nickel oxide
or carbonate. When intensive agitation is used in solutions with
a high nickel concentration, current densities up to 500 asf can
be achieved.
Nickel
coatings from this type of bath usually have very low stress values
and high elongations. Another advantage is that it is possible
to operate the sulfamate bath without difficulties related to
anode dissolution at low chloride levels or even without chloride.
The principle advantage of this bath is that it can be operated
at nickel concentrations of 180-200 g/liter. This allows for the
use of high current densities without losing the properties of
the coating.
Types
of Nickel Plating
Bright
Nickel. Bright
nickel plating baths are used in the automotive, electrical, appliance,
hardware and other industries. Its most important function is
as an undercoating for chromium plating, helping finishers achieve
a smooth bright finish as well as a significant amount of corrosion
protection.
|
Table
IComposition and Operating Parameters
|
|
Nickel
Plating Baths
|
|
Composition
|
Watts
|
High
Chloride
|
All
Chloride
|
Fluoborate
|
Sulfamate*
|
Nickel
Sulfate (oz/gal)
NiSO4 6H2O |
20-40
|
32
|
|
|
|
|
Nickel Chloride (oz/gal)
NiCL2 6H2O
|
6-12
|
12
|
32
|
|
0-3
|
Nickel
Fluoborate (oz/gal)
ni(SO3HN3)2 4H2O |
|
|
|
|
45-60
|
| Boric
Acid (oz/gal) |
4-6
|
4-5
|
4
|
4
|
4-6
|
| pH
Range |
2.0-5.2
|
2.0-2.5
|
0.9-1.1
|
3.0-4.5
|
3.5-4.5
|
| Temperature
(F) |
90-160
|
100-160
|
100-145
|
90-160
|
90-140
|
| Current
Density (asf) |
10-60
|
10-60
|
50-100
|
50-100
|
5-260
|
| Anodes |
Nickel,
bagged, cast rolled, depolarized or carbon type |
| Filtration |
Continuous,
turnover once every 1-4 hr |
| *This
bath is used in electroforming as well as situations where
a low stress/no stress deposit is needed. It allows you to
deposit a lot of nickel in a shorter period of time. The sulfamate
nickel is more expensive than other types of nickel baths. |
Bright
nickel plating baths use combinations of organic agents to achieve
bright nickel deposits. There are two classes of these organic
additives. The first class is the aromatic sulfonic acids, sulfonamides
and sulfonamides that contain the functional group =C-SO-2. Saccharin
is a widely used example of this type of brightener. Nickel deposits
plated using these additives are mirror bright initially; however
as the nickel builds, brightness diminishes. This first class
of brighteners incorporates sulfur into the bright nickel, reducing
corrosion resistance.
Brighteners
in the second class, also called levelers, have inorganic metal
ions and organic compounds. These may include butynediol, coumarin,
ethylene cyanohydrin and formaldehyde. These are used as leveling
agents because they increase surface smoothness as the nickel
deposit thickness increases.
Semi-Bright
Nickel. At first, coumarin was used to obtain a high-leveling,
ductile, semi-bright and sulfur-free nickel deposit from a Watts
nickel bath. However, coumarin-free solutions are now available.
A semi-bright nickel finish is semi-lustrous, as the name implies.
However, it was specifically developed for its ease of polishing
and buffing. Or, if subsequently bright nickel plated, buffing
can be eliminated. Brightness and smoothness are dependent on
operating conditions (see Table I).
The reason semi-bright nickel finishes are so easily buffed and/or
polished is that the structure of the deposit is columnar, whereas
the structure of a bright nickel finish is plate-like (lamellar).
However, the structure can be changed with additives, a change
in pH, current density or even an increase in solution agitation.
This is not a problem unless it affects properties such as internal
stress.
Internal
stress can be compressive or tensile. Compressive stress is where
the deposit expands to relieve the stress. Tensile stress is where
the deposit contracts. Highly compressed deposits can result in
blisters, warping or cause the deposit to separate from the substrate.
Deposits with high tensile stress can also cause warping in addition
to cracking and reduction in fatigue strength.
Watts
baths and high-chloride type baths can produce high tensile stress.
During bright-nickel plating, stress-reducing additives are used,
but these codeposit sulfur materials that affect the physical
and/or engineering properties of the deposit. Saccharin is often
used as a stress reducing agent. Nickel sulfamate baths can deposit
pure low-stressed finishes without using additives.
Other
Types of Nickel. To obtain other types of finishes such as
satin nickel, organic additives are used and deposition conditions
are altered. Deposits from a Watts bath are usually 7-10 mm thick,
with the appearance dependent on the temperature and/or pH. At
higher temperatures and a pH of 4.5-5.0, nickel deposits are matte.
At 122F and a pH of 2.5-3.5, deposits are bright.
Black
nickel plating is lustrous and has a black or dark gray color.
Plating is done with little or no agitation. Occasionally it is
necessary to remove hydrogen gas (bubbles) from the part's surface
using wetting agents. The pH of the bath ranges from 5-6, and
the temperature varies from ambient to 140F. Current density remains
at approximately 0.5 A/dm2.
The
coatings average 2 mm thick and corrosion resistance is limited,
therefore they are usually lacquered or coated with oil or grease.
If the black nickel must have good corrosion resistance, an undercoating
such as bright or dull nickel, zinc or cadmium is necessary.
Barrel
Nickel Plating
Barrel
plating solutions are relatively similar to rack plating solutions;
however, operating conditions may differ, although not radically.
The pH is usually maintained at about 4, unless plating zinc diecasting,
in which case a pH higher than 4 may be necessary. However, anode
corrosion is better at a lower pH, and anode area is limited.
The anode area should be as large as possible to avoid the liberation
of oxygen and chlorine.
Temperatures
can vary for barrel nickel plating from 86-104F for some solutions
and 104-140F for others. Current density can also vary. For a
typical barrel, approximately 24-32 inches long and 16 inches
in diameter, the load is 300-600 amps per load or between 1-1.5
A/dm2. Other considerations are the barrel loading, surface area
and coating thickness.
There
are some special considerations for barrel plating: 1) Parts must
be able to move about freely in the barrel; 2) Precise surface
preparation is essential, including thorough rinsing; and 3) When
the electrolytes are used to full capacity, low-current-density
treatment should be used continuously.
Properties
of Nickel Deposits
Thickness.
Corrosion resistance is often intimately related to the thickness
of the coating; however, the functional requirements of the coating
are also important. Micrometer readings are used most often to
determine coating thickness. ASTM standard B487 describes a method
of measuring coating thickness based on metallographic examination
of cross-section of the plated part. Other ASTM tests include
ASTM B530 and ASTM B504. The ASTM web site (www.astm.org) has
information on the tests mentioned in this article.
Hardness.
Certain addition agents, such as saccharin or napththalene sulfonic
acid, can increase the hardness of a nickel deposit. Wetting agents
may also increase hardness. Nickel deposits plated from Watts
nickel baths, sulfamate or fluoborate baths can rise to 650 HV
(HV is Vickers hardness). Heavy nickel baths produce deposits
with hardnesses between 250-350 HV.
Hardness
is not only a result of addition agents but is also affected by
the plating bath composition, temperature, current density and
other operating conditions. ASTM B578 is a test for the microhardness
of plated coatings.
Ductility.
Ductility can be measured using two ASTM test procedures, B489
and B490. Ductility can also be measured using a tensile testing
machine; however this test is specific to measuring plated thin
foils.
Information
about other properties such as adhesion, brittleness, dull deposits
and burning are covered in PFOnline's Nickel Troubleshooting Guide
which is this month's online exclusive (for the url see the contents
page).
This
primer by no means even scratches the surface of nickel plating.
There have been volumes written on the subject. It is hoped that
this article will give you some information on the basics and
some reference materials as to where you can go to find more information
about the process.