E-Book, Englisch, 464 Seiten
Reihe: Woodhead Publishing Series in Metals and Surface Engineering
Dennis / Such Nickel and Chromium Plating
3. Auflage 1993
ISBN: 978-1-84569-863-8
Verlag: Elsevier Science & Techn.
Format: EPUB
Kopierschutz: 6 - ePub Watermark
E-Book, Englisch, 464 Seiten
Reihe: Woodhead Publishing Series in Metals and Surface Engineering
ISBN: 978-1-84569-863-8
Verlag: Elsevier Science & Techn.
Format: EPUB
Kopierschutz: 6 - ePub Watermark
During the last decade the engineering applications for nickel and chromium coatings have gained in importance. In this third edition the chapter dealing with engineering applications has been updated and expanded to include more information on electroforming and composite coatings, and engineering applications have been emphasised in the additions to the chapter on autocatalytic deposition of nickel. Additions have been made to the sections on pulse plating and use or rotating cathodes, and the section on trivalent chromium has been extended.
Autoren/Hrsg.
Weitere Infos & Material
1;Front Cover;1
2;Nickel and Chromium Plating;4
3;Copyright Page;5
4;Table of Contents;6
5;Preface to the first edition;9
6;Preface to the second edition;11
7;Preface to the third edition;13
8;Chapter 1. Introduction and historical review;16
8.1;History of nickel plating;19
8.2;History of chromium plating;24
8.3;The future of nickel and chromium plating;26
8.4;References;26
8.5;Bibliography;27
9;Chapter 2. Metallurgical aspects of electrodeposition;28
9.1;Methods of examination of stucture and surface topography;28
9.2;References;54
9.3;Bibliography;54
10;Chapter 3. Electroplating baths and anodes used for industrial nickel deposition;56
10.1;Plating baths;56
10.2;Anodes for nickel plating;62
10.3;Barrel nickel plating;72
10.4;Health hazards caused by nickel plating;76
10.5;References;78
10.6;Bibliography;80
11;Chapter 4. Engineering applications;81
11.1;Applications of thick electrodeposits;81
11.2;Chromium electrodeposits;104
11.3;References;109
11.4;Bibliography;110
12;Chapter 5. Bright nickel electroplating;111
12.1;Brighteners;111
12.2;Properties of electrodeposited bright nickel;119
12.3;Properties of bright nickel baths;127
12.4;The incorporation and effect of organic addition agents;131
12.5;References;145
12.6;Bibliography;146
13;Chapter 6. Control and purification of nickel electroplating solutions;147
13.1;Control of inorganic constituents;147
13.2;Control of organic constituents;148
13.3;Common contaminants of nickel plating baths;150
13.4;Effect of metallic contamination on structure and properties of nickel deposits;154
13.5;Analysis for inorganic impurities;167
13.6;Removal of metallic contamination;168
13.7;Types of organic contamination;170
13.8;Filtration of electroplating baths;173
13.9;References;175
14;Chapter 7. Physical and mechanical properties of electrodeposits and methods of determination;177
14.1;Ductility;177
14.2;Adhesion;184
14.3;Stress;195
14.4;Hardness and wear resistance;209
14.5;Assessment of surface quality - brightness, reflectivity and surface roughness;213
14.6;References;217
14.7;Bibliography;219
15;Chapter 8. Chromium plating;220
15.1;The mechanism of deposition from chromic acid plating baths;221
15.2;Baths based on chromic acid;222
15.3;Electrodeposition from trivalent baths;239
15.4;Stress in chromium deposits;245
15.5;Barrel chromium plating;253
15.6;Health hazards of chromium plating;255
15.7;References;256
15.8;Bibliography;259
16;Chapter 9. Thickness and corrosion testing of nickel plus chromium coatings;260
16.1;Thickness testing;260
16.2;Corrosion testing;266
16.3;Methods of evaluation of corrosion results;272
16.4;References;282
16.5;Bibliography;284
17;Chapter 10. Decorative nickel plus chromium coating combinations;285
17.1;Multi-layer nickel coatings;288
17.2;Satin nickel;296
17.3;Modification of the chromium layer;297
17.4;Evaluation of corrosion resistance of nickel plus chromium coatings;311
17.5;Corrosion resistance of deformed nickel plus chromium coatings;317
17.6;References;322
18;Chapter 11. Autocatalytic deposition of nickel;325
18.1;Phosphorus alloys;329
18.2;Pure autocatalytic nickel;338
18.3;Autocatalytic nickel coatings with non-metallic inclusions;339
18.4;References;342
18.5;Bibliography;344
19;Chapter 12. Electroplating onto plastics;345
19.1;Electroplating onto plastics other than ABS;356
19.2;Testing of plated plastics;359
19.3;References;375
20;Chapter 13. Deposition of nickel alloys;378
20.1;Nickel/cobalt alloys;378
20.2;Nickel/iron alloys;383
20.3;Nickel/tin alloys;388
20.4;Nickel/molybdenum and nickel/tungsten alloys;389
20.5;Nickel/phosphorus alloys;391
20.6;Autocatalytic nickel polyalloys;391
20.7;Nickel/manganese alloys;392
20.8;Nickel/chromium alloys;393
20.9;Nickel/indium alloys;394
20.10;Nickel/copper alloys;394
20.11;Miscellaneous alloys;395
20.12;References;402
20.13;Bibliography;404
21;Chapter 14. Plating on difficult-to-plate metals;405
21.1;Aluminium;405
21.2;Preparation of uncommon metals for nickel plating;426
21.3;References;435
21.4;Bibliography;437
22;Chapter 15. High-speed plating;438
22.1;Electrochemical factors;438
22.2;Plating solution composition;442
22.3;Methods used to increase the rate of deposition;442
22.4;Brush plating;448
22.5;Abrasive plating;451
22.6;Properties of deposits plated at high current density;453
22.7;References;455
22.8;Bibliography;456
23;Index;457
Chapter 1 Introduction and historical review
Electrodeposited metals are often an ideal means of providing a thin surface coating which has some property (or properties) superior to that of the substrate. It may, for example, be possible to employ a cheaper or stronger substrate than could otherwise be used and yet achieve good corrosion resistance by applying a suitable electrodeposited coating. Electrodeposited nickel is typical of metals which can be included in the above category. It is often applied for decorative and protective purposes to cheap mild steel pressings and to die-cast zinc or aluminium alloy components. Die-casting is an economical means of mass-producing exact dimensional replicates of the original, but the alloys used are not suitable for service in a corrosive atmosphere without some form of protective coating. About 90% of the estimated 75 000t of nickel consumed during 1990 in the electroplating industries of non-communist countries was used in the form of thin, corrosion resistant and often decorative coatings on cheaply produced or strong substrates. This quantity excludes that consumed for plating in those countries which were part of the former USSR and also in China, as statistics are almost impossible to obtain. Most nickel coatings of this type are subsequently chromium plated to form the familiar composite nickel plus chromium system. While nickel coatings may be applied solely for corrosion resistance where their inherent dullness is of no importance, the majority have to provide both decorative and protective functions. If a final bright appearance is required, dull deposits have to be polished to a high lustre before chromium plating and, since this polishing operation is very expensive, the major part of nickel plated for decorative applications has for many years been deposited in a fully-bright condition. Such coatings are obtained from solutions which contain organic chemicals in addition to the inorganic constituents. Not only can these additions modify the structure of the nickel deposit so that polishing is unnecessary, but many also have scratch-filling (the so-called ‘levelling’) properties which also eliminate or reduce the amount of polishing of the basis metal which is required. Variants of these solutions give bright, levelling deposits and form the vast majority of nickel baths now in industrial use. However, it is not the authors’ intention to minimize the importance of the remaining uses of nickel electrodeposition. Indeed, these are of great and increasing economic importance. Often a comparatively thin nickel coating of which the weight and cost expressed as anode metal are quite small, may be used to repair a most expensive component which would otherwise have to be scrapped. Large engineering components which have involved much costly machining and heat-treatment, and have been damaged, worn or over-machined, perhaps only on small portions of their surface, can be salvaged by building up these specific portions with nickel to restore their original dimensions. If a large nickel thickness is necessary, this reclamation involves the deposition of more nickel than required, followed by machining to size. Obviously, the economics of these operations must be compared with those of fabricating an entirely new component. The benefits conferred on the surface by thick or ‘heavy’ nickel plate are not only better corrosion protection, but also the greater abrasion resistance obtainable from certain types of nickel coatings. These advantages are now utilized on many new as well as reclaimed parts; this is discussed in Chapter 4. The superior wear-resistant properties of these nickel electrodeposits are often further enhanced by the deposition of fairly thick chromium coatings. This is the ‘hard’ chromium plate of the engineer. Electroforming is the fabrication of articles entirely by electrodeposition. Nickel is a popular metal for this purpose since it can be plated in a ductile and low stressed form which has moderate hardness. Electroforms which have higher hardness and strength, both at ambient and elevated temperatures, can be produced from special solutions from which are deposited nickels whose structure is modified either by inorganic or organic chemicals present in the electroplating bath or by containing other metals as alloying ingredients. The working surface of the electroform may be chromium plated after removal from the mandrel. Sometimes the thick skin of the electroform is backed by even thicker copper plate, which although softer than nickel, can be deposited at a faster rate than can most types of nickel. Alternative and even faster means of applying a backing material to the electroformed nickel shell are by casting a low melting point alloy into it or by flame-spraying of a suitable alloy having a higher melting-point. Large electroformed ‘skins’ can be supported by filling with concrete. These are frequently used as tools for moulding large vehicle panels from plastics materials. The functional uses of nickel whether as electroplated coatings or electroformed artefacts are growing steadily, as the advantages of this metal in its naturally electrodeposited form or as modified by various techniques become evident to design and production engineers. As described in Chapter 4, this versatility enables electroformed dies to be used for casting metals and glass, in addition to moulding plastics. The use of nickel for electroforming mesh is also a growth industry, for this mesh according to its hole dimensions and shapes can be used for a wide variety of applications. The world market for electroformed nickel has increased substantially in the last two decades and appears likely to continue to grow. This increase has partly compensated for the decreased use of nickel electroplate in its traditional form as a bright coating. This decrease is partly due to the decline in world industrial output only too evident at the time of writing, but was occurring before the current trade recession commenced. The number and size of bright finished components on individual cars and domestic durables had been deliberately reduced as a policy. This policy was partly influenced by a wish to change to black or coloured finishes but also as a result of attempts to lower the costs of finishing. The combination of these factors has produced a serious decrease in the use of nickel electroplate for decorative coatings in Europe and North America. However, the total world usage of nickel for electroplating has increased during the last decade because of greater consumption in the developing countries of Asia. It will be noted that for most decorative/corrosion protective purposes, many engineering uses and sometimes when electroformed, electrodeposited nickel is given a top coat of chromium. For this reason, it is impossible to dissociate chromium electrodeposition from that of nickel. Therefore, although the main purpose of this text is to discuss the deposition of nickel, the technology of chromium plating is discussed wherever it is relevant. The chief emphasis is on electrodeposition of nickel, but Chapter 11 describes the autocatalytic plating of chemically reduced nickel (electroless nickel), as this is a valuable and increasingly used technique for applying uniform coatings to articles of complex shape, where the inherent limitations of the electrolytic process form an impossible barrier to obtaining a uniform coating of nickel over the whole surface. The properties of the nickel alloys deposited can also be advantageous. Accordingly, the industrial use of electroless nickel, especially the nickel/phosphorus alloy, has grown steadily during the last decade because of its unique properties. The science of electroplating is about 180 years old. Nickel was first deposited 150 years ago and chromium some 20 years later, but chromium has only been used as an overlay in decorative nickel plus chromium coatings since the late 1920s. However, the great advances in nickel technology have been achieved only in the last 70 years, and these and the early pioneering work form a fascinating historical introduction to the present processes used in industry. History of nickel plating
The electrodeposition of nickel was first described in 1837. G. Bird1 electrolysed solutions of nickel chloride or sulphate for some hours and so obtained a crust of metallic nickel on a platinum electrode. In 1840, the first patent for commercial nickel plating was granted to J. Shore2 of England who specified a solution of nickel nitrate. Soon afterwards a number of investigators published the results of their experiments. A. Smee of England (1841), Ruolz of France (1843) and Bottger of Germany (1843) were the first of these. Ruolz used nickel chloride or nitrate but Bottger’s was the first publication to mention an electrolyte solution based on ‘acid ammonium sulphate’; this bath, with variations, was the one mainly used in commerce for the next 70 years. However, G. Gore (1855) seems to have been the first to publish3 details of the neutral nickel ammonium sulphate bath (nickel ammonium sulphate is colloquially known as double nickel salts). Becquerel also published the process in 1862, using a concentration of 70–80g/l, although it is possible he used an excess of ammonia. Therefore, undue credit has perhaps been given to Dr I. Adams of the USA for developing this process, although he did apparently use it in the laboratory at Harvard University in 1858–18604. However, he certainly appears to have been the first to commercialize it by plating gas burner tips in...