Contact Materials for Electrical Engineering
Contents
Introduction
The contact parts are important components in switching devices. They have to maintain their function from the new state until the end of the functional life of the devices.
The requirements on contacts are rather broad. Besides typical contact properties such as
- High arc erosion resistance
- High resistance against welding
- Low contact resistance
- Good arc moving properties
- Good arc extinguishing capability
they have to exhibit physical, mechanical, and chemical properties like high electrical and thermal conductivity, high hardness, high corrosion resistance, etc and besides this should have good mechanical workability, and also be suitable for good weld and brazing attachment to contact carriers. In addition they must be made from environmentally friendly materials.
Materials suited for use as electrical contacts can be divided into the following groups based on their composition and metallurgical structure:
- Pure metals
- Alloys
- Composite materials
- Pure metals
From this group silver has the greatest importance for switching devices in the higher energy technology. Other precious metals such as gold and platinum are only used in applications for the information technology in the form of thin surface layers. As a nonprecious metal tungsten is used for some special applications such as for example as automotive horn contacts. In some rarer cases pure copper is used but mainly paired to a silver-based contact material.
- Alloys
Besides these few pure metals a larger number of alloy materials made by melt technology are available for the use as contacts. An alloy is characterized by the fact that its components are completely or partially soluble in each other in the solid state. Phase diagrams for multiple metal compositions show the number and type of the crystal structure as a function of the temperature and composition of the alloying components.
They indicate the boundaries of liquid and solid phases and define the parameters of solidification. Alloying allows to improve the properties of one material at the cost of changing them for the second material. As an example, the hardness of a base metal may be increased while at the same time the electrical conductivity decreases with even small additions of the second alloying component.
- Composite Materials
Composite materials are a material group whose properties are of great importance for electrical contacts that are used in switching devices for higher electrical currents. Those used in electrical contacts are heterogeneous materials composed of two or more uniformly dispersed components in which the largest volume portion consists of a metal. The properties of composite materials are determined mainly independent from each other by the properties of their individual components. Therefore it is for example possible to combine the high melting point and arc erosion resistance of tungsten with the low melting and good electrical conductivity of copper, or the high conductivity of silver with the weld resistant metalloid graphite.
Figure 2.1 shows the schematic manufacturing processes from powder blending to contact material. Three basic process variations are typically applied:
- Sintering without liquid phase (Press-Sinter-Repress, PSR)
- Sintering with liquid phase
- Infiltration (Press-Sinter-Infiltrate, PSI)
During sintering without a liquid phase (left side of schematic) the powder mix is first densified by pressing, then undergoes a heat treatment (sintering), and eventually is re-pressed again to further increase the density. The sintering atmosphere depends on the material components and later application; a vacuum is used for example for the low gas content material Cu/Cr. This process is used for individual contact parts and also termed press-sinterrepress (PSR). For materials with high silver content the starting point at pressing is most a larger block (or billet) which is then after sintering hot extruded into wire, rod, or strip form. The extrusion further increases the density of these composite materials and contributes to higher arc erosion resistance. Materials such as Ag/Ni, Ag/MeO, and Ag/C are typically produced by this process.
Sintering with liquid phase has the advantage of shorter process times due to the accelerated diffusion and also results in near-theoretical densities of the
Fig. 2.1: Powder-metallurgical manufacturing of composite materials (schematic) T = Melting point of the lower melting component
composite material. To ensure the shape stability during the sintering process it is however necessary to limit the volume content of the liquid phase material.
As opposed to the liquid phase sintering which has limited use for electrical contact manufacturing, the Infiltration process as shown on the right side of the schematic has a broad practical range of applications. In this process the powder of the higher melting component sometimes also as a powder mix with a small amount of the second material is pressed into parts and after sintering the porous skeleton is infiltrated with liquid metal of the second material. The filling up of the pores happens through capillary forces. This process reaches after the infiltration near-theoretical density without subsequent pressing and is widely used for Ag- and Cu-refractory contacts. For Ag/W or Ag/WC contacts, controlling the amount or excess on the bottom side of the contact of the infiltration metal Ag results in contact tips that can be easily attached to their carriers by resistance welding. For larger Cu/W contacts additional machining is often used to obtain the final shape of the contact component.
Gold Based Materials
Pure Gold is besides Platinum the chemically most stable of all precious metals. In its pure form it is not very suitable for use as a contact material in electromechanical devices because of its tendency to stick and cold-weld at even low contact forces. In addition it is not hard or strong enough to resist mechanical wear and exhibits high materials losses under electrical arcing loads. This limits its use in form of thin electroplated or vacuum deposited layers.
For most electrical contact applications gold alloys are used. Depending on the alloying metal the melting is performed either under in a reducing atmosphere or in a vacuum. The choice of alloying metals depends on the intended use of the resulting contact material. The binary Au alloys with typically <10 wt% of other precious metals such as Pt, Pd, or Ag or non-precious metals like Ni, Co, and Cu are the more commonly used ones (Table 2.2). On one hand these alloy additions improve the mechanical strength and electrical switching properties but on the other hand reduce the electrical conductivity and chemical corrosion resistance (Fig. 2.2) to varying degrees.
Under the aspect of reducing the gold content ternary alloys with a gold content of approximately 70 wt% and additions of Ag and Cu or Ag and Ni resp., for example AuAg25Cu5 or AuAg20Cu10 are used which exhibit for many applications good mechanical stability while at the same time have sufficient resistance against the formation of corrosion layers (Table 2.3). Other ternary alloys based on the AuAg system are AuAg26Ni3 and AuAg25Pt6. These alloys are mechanically similar to the AuAgCu alloys but have significantly higher oxidation resistance at elevated temperatures (Table 2.4).
Caused by higher gold prices over the past years the development of alloys with further reduced gold content had a high priority. The starting point has been the AuPd system which has continuous solubility of the two components. Besides the binary alloy of AuPd40 and the ternary one AuPd35Ag9 other multiple component alloys were developed. These alloys typically have < 50 wt% Au and often can be solution hardened in order to obtain even higher hardness and tensile strength. They are mostly used in sliding contact applications.
Gold alloys are used in the form of welded wire or profile (also called weldtapes), segments, contact rivets, and stampings produced from clad strip materials. The selection of the bonding process is based on the cost for the joining process, and most importantly on the economical aspect of using the least possible amount of the expensive precious metal component.
Besides being used as switching contacts in relays and pushbuttons, gold alloys are also applied in the design of connectors as well as sliding contacts for potentiometers, sensors, slip rings, and brushes in miniature DC motors (Table 2.5).
Table 2.3: Mechanical Properties of Gold and Gold-Alloys
Table 2.1: Commonly Used Grades of Gold
Table 2.2: Physical Properties of Gold and Gold-Alloys
Fig. 2.2: Influence of 1-10 atomic% of different alloying metals on the electrical resistivity of gold (according to J. O. Linde)
Fig. 2.3: Phase diagram of goldplatinum
Fig. 2.4: Phase diagram of gold-silver
Fig. 2.5: Phase diagram of gold-copper
Fig. 2.6: Phase diagram of gold-nickel
Fig. 2.7: Phase diagram of gold-cobalt
Fig. 2.8: Strain hardening of Au by cold working
Fig. 2.9: Softening of Au after annealing for 0.5 hrs after 80% cold working
Fig. 2.10: Strain hardening of AuPt10 by cold working
Fig. 2.11: Strain hardening of AuAg20 by cold working
Fig. 2.12: Strain hardening of AuAg30 by cold working
Fig. 2.13: Strain hardening of AuNi5 by cold working
Fig. 2.14: Softening of AuNi5 after annealing for 0.5 hrs after 80% cold working
Fig. 2.15: Strain hardening of AuCo5 by cold working
Fig. 2.16: Precipitation hardening of AuCo5 at 400°C hardening temperature
Fig. 2.17: Strain hardening of AuAg25Pt6 by cold working
Fig. 2.18: Strain hardening of AuAg26Ni3 by cold working
Fig. 2.19: Softening of AuAg26Ni3 after annealing for 0.5 hrs after 80% cold working
Fig. 2.20: Strain hardening of AuAg25Cu5 by cold working
Fig. 2.21: Strain hardening of AuAg20Cu10 by cold working
Fig. 2.22: Softening of AuAg20Cu10 after annealing for 0.5 hrs after 80% cold working
Fig. 2.23: Strain hardening of AuCu14Pt9Ag4 by cold working
Fig. 2.24: Precipitation hardening of AuCu14Pt9Ag4 at different hardening temperatures after 50% cold working
Table 2.4: Contact and Switching Properties of Gold and Gold Alloys
Table 2.5: Application Examples and Forms of Gold and Gold Alloys
Platinum Metal Based Materials
The platinum group metals include the elements Pt, Pd, Rh, Ru, Ir, and Os (Table 2.6). For electrical contacts platinum and palladium have practical significance as base alloy materials and ruthenium and iridium are used as alloying components. Pt and Pd have similar corrosion resistance as gold but because of their catalytical properties they tend to polymerize adsorbed organic vapors on contact surfaces. During frictional movement between contact surfaces the polymerized compounds known as “brown powder” are formed which can lead to significantly increase in contact resistance. Therefore Pt and Pd are typically used as alloys and not in their pure form for electrical contact applications.
Rhodium is not used as a solid contact material but is applied for example as a electroplated layer in sliding contact systems. Ruthenium is mostly used as an alloying component in the material PdRu15. The metals osmium and iridium have no practical applications in electrical contacts.
Since Pd was for the longest time rather stable in price it was looked at as a substitute for the more expensive gold. This was followed by a steep increase in the Pd price which caused a significant reduction in its use in electrical contacts. Today (2011) the Pd price again is lower than that of gold.
Alloys of Pt with Ru, Ir, Ni, and W were widely used in electromechanical components in the telecommunication industry and in heavy duty automotive breaker points (Table 2.7). Today these components have been replaced in many applications by solid state technology and the usage of these materials is greatly reduced. Pd alloys however have a more significant importance. PdCu15 is widely used for example in automotive flasher relays. Because of their resistance to sulfide formation PdAg alloys are applied in various relay designs. The ability to thermally precipitation harden some multi component alloys based on PdAgAuPt they find special usage in wear resistant sliding contact applications. Pd44Ag38Cu15PtAuZn is a standard alloy in this group.
Platinum and palladium alloys are mainly used similar to the gold based materials in the form of welded wire and profile segments but rarely as contact rivets. Because of the high precious metal prices joining technologies are used that allow the most economic application of the contact alloy in the area where functionally needed. Because of their resistance to material transfer they are used for DC applications and due to their higher arc erosion resistance they are applied for medium electrical loads up to about 30W in relays and switches (Table 2.10). Multi-component alloys based on Pd with higher hardness and wear resistance are mainly used as spring arms in sliding contact systems and DC miniature motors.
Table 2.6: Properties, Production Processes, and Application Forms for Platinum Metals
Table 2.7: Physical Properties of the Platinum Metals and their Alloys
Table 2.8: Mechanical Properties of the Platinum Metals and their Alloys
Fig. 2.25: Influence of 1- 20 atom% of different additive metals on the electrical resistivity p of platinum (Degussa)
Fig. 2.26: Influence of 1-22 atom% of different additive metals on the electrical resistivity p of palladium
Fig. 2.27: Phase diagram of platinum-iridium
Fig. 2.28: Phase diagram of platinum-nickel
Fig. 2.29: Phase diagram of platinum-tungsten
Fig. 2.30: Phase diagram of palladium-copper
Fig. 2.31: Strain hardening of Pt by cold working
Fig. 2.32: Softening of Pt after annealing for 0.5 hrs after 80% cold working
Fig. 2.33: Strain hardening of PtIr5 by cold working
Fig. 2.34: Softening of PtIr5 after annealing for 1 hr after different degrees of cold working
Fig. 2.35: Strain hardening of PtNi8 by cold working
Fig. 2.36: Softening of PtNi8 after annealing for 1 hr after 80% cold working
Fig. 2.37: Strain hardening of PtW5 by cold working
Fig. 2.38: Softening of PtW5 after annealing for 1hr after 80% cold working
Fig. 2.39: Strain hardening of Pd 99.99 by cold working
Fig. 2.40: Strain hardening of PdCu15 by cold working
Fig. 2.41: Softening of PdCu15 after annealing for 0.5 hrs
Fig. 2.42: Strain hardening of PdCu40 by cold working
Fig. 2.43: Softening of PdCu40 after annealing for 0.5 hrs after 80% cold working
Fig. 2.44: Electrical resistivity p of PdCu alloys with and without an annealing step for forming an ordered phase
Table 2.9: Contact and Switching Properties of the Platinum Metals and their Alloys
Table 2.10: Application Examples and Form of Supply for Platinum Metals and their Alloys
Silver Based Materials
Pure Silver
Pure silver (also called fine silver) exhibits the highest electrical and thermal conductivity of all metals. It is also resistant against oxidation. Major disadvantages are its low mechanical wear resistance, the low softening temperature, and especially its strong affinity to sulfur and sulfur compounds. In the presence of sulfur and sulfur containing compounds brownish to black silver sulfide layer are formed on its surface. These can cause increased contact resistance or even total failure of a switching device if they are not mechanically, electrically, or thermally destroyed. Other weaknesses of silver contacts are the tendency to weld under the influence of over-currents and the low resistance against material transfer when switching DC loads. In humid environments and under the influence of an electrical field silver can creep (silver migration) and cause electrical shorting between adjacent current paths.
Table 2.11 shows the typically available quality grades of silver. In certain economic areas, i.e. China, there are additional grades with varying amounts of impurities available on the market. In powder form silver is used for a wide variety of silver based composite contact materials. Different manufacturing processes result in different grades of Ag powder as shown in Table 2.12. additional properties of silver powders and their usage are described in chapter 8.1. Semi-finished silver materials can easily be warm or cold formed and can be clad to the usual base materials. For attachment of silver to contact carrier materials welding of wire or profile cut-offs and brazing are most widely applied. Besides these mechanical processes such as wire insertion (wire staking) and the riveting (staking) of solid or composite contact rivets are used in the manufacture of contact components.
Contacts made from fine silver are applied in various electrical switching devices such as relays, pushbuttons, appliance and control switches for currents < 2 A (Table 2.16). Electroplated silver coatings are widely used to reduce the contact resistance and improve the brazing behavior of other contact materials and components.
Table 2.11: Overview of the Most Widely Used Silver Grades
Table 2.12: Quality Criteria of Differently Manufactured Silver Powders
Fig. 2.45: Strain hardening of Ag 99.95 by cold working
Fig. 2.46: Softening of Ag 99.95 after annealing for 1 hr after different degrees of strain hardening
Silver Alloys
To improve the physical and contact properties of fine silver melt-metallurgical produced silver alloys are used (Table 2.13). By adding metal components the mechanical properties such as hardness and tensile strength as well as typical contact properties such as erosion resistance, and resistance against material transfer in DC circuits are increased (Table 2.14). On the other hand however, other properties such as electrical conductivity and chemical corrosion resistance can be negatively impacted by alloying (Figs. 2.47 and 2.48).
Fine-Grain Silver
Fine-Grain Silver (ARGODUR-Spezial) is defined as a silver alloy with an addition of 0.15 wt% of Nickel. Silver and nickel are not soluble in each other in solid form. In liquid silver only a small amount of nickel is soluble as the phase diagram (Fig. 2.51) illustrates. During solidification of the melt this nickel addition gets finely dispersed in the silver matrix and eliminates the pronounce coarse grain growth after prolonged influence of elevated temperatures (Figs. 2.49 and 2.50).
Fine-grain silver has almost the same chemical corrosion resistance as fine silver. Compared to pure silver it exhibits a slightly increased hardness and tensile strength (Table 2.14). The electrical conductivity is just slightly decreased by this low nickel addition. Because of its significantly improved contact properties fine grain silver has replaced pure silver in many applications.
Hard-Silver Alloys
Using copper as an alloying component increases the mechanical stability of silver significantly. The most important among the binary AgCu alloys is that of AgCu3, known in europe also under the name of hard-silver. This material still has a chemical corrosion resistance close to that of fine silver. In comparison to pure silver and fine-grain silver AgCu3 exhibits increased mechanical strength as well as higher arc erosion resistance and mechanical wear resistance (Table 2.14).
Increasing the Cu content further also increases the mechanical strength of AgCu alloys and improves arc erosion resistance and resistance against material transfer while at the same time however the tendency to oxide formation becomes detrimental. This causes during switching under arcing conditions an increase in contact resistance with rising numbers of operation. In special applications where highest mechanical strength is recommended and a reduced chemical resistance can be tolerated, the eutectic AgCu alloy with 28 wt% of copper (Fig. 2.52) is used. AgCu10 also known as coin silver has been replaced in many applications by composite silver-based materials while sterling silver (AgCu7.5) has never extended its important usage from decorative table wear and jewelry to industrial applications in electrical contacts.
Besides these binary alloys, ternary AgCuNi alloys are used in electrical contact applications. From this group the material ARGODUR 27, an alloy of 98 wt% Ag with a 2 wt% Cu and nickel addition has found practical importance close to that of AgCu3. This material is characterized by high resistance to oxidation and low tendency to re-crystallization during exposure to high temperatures. Besides high mechanical stability this AgCuNi alloy also exhibits a strong resistance against arc erosion. Because of its high resistance against material transfer the alloy AgCu24.5Ni0.5 has been used in the automotive industry for an extended time in the North American market. Caused by miniaturization and the related reduction in available contact forces in relays and switches this material has been replaced widely because of its tendency to oxide formation.
The attachment methods used for the hard silver materials are mostly close to those applied for fine silver and fine grain silver.
Hard-silver alloys are widely used for switching applications in the information and energy technology for currents up to 10 A, in special cases also for higher current ranges (Table 2.16).
Dispersion hardened alloys of silver with 0.5 wt% MgO and NiO (ARGODUR 32) are produced by internal oxidation. While the melt-metallurgical alloy is easy to cold-work and form the material becomes very hard and brittle after dispersion hardening. Compared to fine silver and hard-silver this material has a greatly improved temperature stability and can be exposed to brazing temperatures up to 800°C without decreasing its hardness and tensile strength. Because of these mechanical properties and its high electrical conductivity
Table 2.13: Physical Properties of Silver and Silver Alloys
ARGODUR 32 is mainly used in the form of contact springs that are exposed to high thermal and mechanical stresses in relays, and contactors for aeronautic applications.
Fig. 2.47: Influence of 1-10 atom% of different alloying metals on the electrical resistivity of silver
Fig. 2.48: Electrical resistivity p of AgCu alloys with 0-20 weight% Cu in the soft annealed and tempered stage a) Annealed and quenched b) Tempered at 280°C
Fig. 2.49: Coarse grain micro structure of Ag 99.97 after 80% cold working and 1 hr annealing at 600°C
Fig. 2.50: Fine grain microstructure of AgNi0.15 after 80% cold working and 1 hr annealing at 600°C
Fig. 2.51: Phase diagram of silver-nickel
Fig. 2.52: Phase diagram of silver-copper
Fig. 2.53: Phase diagram of silver-cadmium
Table 2.14: Mechanical Properties of Silver and Silver Alloys
Fig. 2.54: Strain hardening of AgCu3 by cold working
Fig. 2.55: Softening of AgCu3 after annealing for 1 hr after 80% cold working
Fig. 2.56: Strain hardening of AgCu5 by cold working
Fig. 2.57: Softening of AgCu5 after annealing for 1 hr after 80% cold working
Fig. 2.58: Strain hardening of AgCu 10 by cold working
Fig. 2.59: Softening of AgCu10 after annealing for 1 hr after 80% cold working
Fig. 2.60: Strain hardening of AgCu28 by cold working
Fig. 2.61: Softening of AgCu28 after annealing for 1 hr after 80% cold working
Fig. 2.62: Strain hardening of AgNi0.15 by cold working
Fig. 2.63: Softening of AgNi0.15 after annealing for 1 hr after 80% cold working
Fig. 2.64: Strain hardening of ARGODUR 27 by cold working
Fig. 2.65: Softening of ARGODUR 27 after annealing for 1 hr after 80% cold working
Table 2.15: Contact and Switching Properties of Silver and Silver Alloys
Table 2.16: Application Examples and Forms of Supply for Silver and Silver Alloys
Silver-Palladium Alloys
The addition of 30 wt% Pd increases the mechanical properties as well as the resistance of silver against the influence of sulfur and sulfur containing compounds significantly (Tables 2.17 and 2.18). Alloys with 40-60 wt% Pd have an even higher resistance against silver sulfide formation. At these percentage ranges however the catalytic properties of palladium can influence the contact resistance behavior negatively. The formability also decreases with increasing Pd contents.
AgPd alloys are hard, arc erosion resistant, and have a lower tendency towards material transfer under DC loads (Table 2.19). On the other hand the electrical conductivity is decreased at higher Pd contents. The ternary alloy AgPd30Cu5 has an even higher hardness which makes it suitable for use in sliding contact systems.
AgPd alloys are mostly used in relays for the switching of medium to higher loads (>60V, >2A) as shown in Table 2.20. Because of the high palladium price these formerly solid contacts have been widely replaced by multi-layer designs such as AgNi0.15 or AgNi10 with a thin Au surface layer. A broader field of application for AgPd alloys remains in the wear resistant sliding contact systems.
Fig. 2.66: Phase diagram of silver-palladium
Fig. 2.67: Strain hardening of AgPd30 by cold working
Fig. 2.68: Strain hardening of AgPd50 by cold working
Fig. 2.69: Strain hardening of AgPd30Cu5 by cold working
Fig. 2.70: Softening of AgPd30, AgPd50, and AgPd30Cu5 after annealing of 1 hr after 80% cold working
Table 2.17: Physical Properties of Silver-Palladium Alloys
Table 2.18: Mechanical Properties of Silver-Palladium Alloys
Table 2.19: Contact and Switching Properties of Silver-Palladium Alloys
Table 2.20: Application Examples and Forms of Suppl for Silver-Palladium Alloys
Silver Composite Materials
Silver-Nickel (SINIDUR) Materials
Since silver and nickel are not soluble in each other in solid form and in the liquid phase have only very limited solubility silver nickel composite materials with higher Ni contents can only be produced by powder metallurgy. During extrusion of sintered Ag/Ni billets into wires, strips and rods the Ni particles embedded in the Ag matrix are stretched and oriented in the microstructure into a pronounced fiber structure (Figs. 2.75. and 2.76)
The high density produced during hot extrusion aids the arc erosion resistance of these materials (Tables 2.21 and 2.22). The typical application of Ag/Ni contact materials is in devices for switching currents of up to 100A (Table 2.24). In this range they are significantly more erosion resistant than silver or silver alloys. In addition they exhibit with nickel contents <20 wt% a low and over their operational lifetime consistent contact resistance and good arc moving properties. In DC applications Ag/Ni materials exhibit a relatively low tendency of material transfer distributed evenly over the contact surfaces (Table 2.23).
Typically Ag/Ni (SINIDUR) materials are usually produced with contents of 10-40 wt% Ni. The most widely used materials SINIDUR 10 and SINIDUR 20- and also SINIDUR 15, mostly used in north america-, are easily formable and applied by cladding (Figs. 2.71-2.74). They can be, without any additional welding aids, economically welded and brazed to the commonly used contact carrier materials. The (SINIDUR) materials with nickel contents of 30 and 40 wt% are used in switching devices requiring a higher arc erosion resistance and where increases in contact resistance can be compensated through higher contact forces.
The most important applications for Ag/Ni contact materials are typically in relays, wiring devices, appliance switches, thermostatic controls, auxiliary switches, and small contactors with nominal currents >20A (Table 2.24).
Table 2.21: Physical Properties of Silver-Nickel (SINIDUR) Materials
Table 2.22: Mechanical Properties of Silver-Nickel (SINIDUR) Materials
Fig. 2.71: Strain hardening of Ag/Ni 90/10 by cold working
Fig. 2.72: Softening of Ag/Ni 90/10 after annealing for 1 hr after 80% cold working
Fig. 2.73: Strain hardening of Ag/Ni 80/20 by cold working
Fig. 2.74: Softening of Ag/Ni 80/20 after annealing for 1 hr after 80% cold working
Fig. 2.75: Micro structure of Ag/Ni 90/10 a) perpendicular to the extrusion direction b) parallel to the extrusion direction
Fig. 2.76: Micro structure of Ag/Ni 80/20 a) perpendicular to the extrusion direction b) parallel t o the extrusion direction
Table 2.23: Contact and Switching Properties of Silver-Nickel (SINIDUR) Materials
Table 2.24: Application Examples and Forms of Supply for Silver-Nickel (SINIDUR) Materials
Silver-Metal Oxide Materials Ag/CdO, Ag/SnO2, Ag/ZnO
The family of silver-metal oxide contact materials includes the material groups: silver-cadmium oxide (DODURIT CdO), silver-tin oxide (SISTADOX), and silverzinc oxide (DODURIT ZnO). Because of their very good contact and switching properties like high resistance against welding, low contact resistance, and high arc erosion resistance, silver-metal oxides have gained an outstanding position in a broad field of applications. They mainly are used in low voltage electrical switching devices like relays, installation and distribution switches, appliances, industrial controls, motor controls, and protective devices (Table 2.13).
- Silver-cadmium oxide (DODURIT CdO) materials
Silver-cadmium oxide (DODURIT CdO) materials with 10-15 wt% are produced by both, internal oxidation and powder metallurgical methods (Table 2.25).
The manufacturing of strips and wires by internal oxidation starts with a molten alloy of silver and cadmium. During a heat treatment below it's melting point in a oxygen rich atmosphere in such a homogeneous alloy the oxygen diffuses from the surface into the bulk of the material and oxidizes the Cd to CdO in a more or less fine particle precipitation inside the Ag matrix. The CdO particles are rather fine in the surface area and are becoming larger further away towards the center of the material (Fig. 2.83).
During the manufacturing of Ag/CdO contact material by internal oxidation the processes vary depending on the type of semi-finished material. For Ag/CdO wires a complete oxidation of the AgCd wire is performed, followed by wire-drawing to the required diameter (Figs. 2.77 and 2.78). The resulting material is used for example in the production of contact rivets. For Ag/CdO strip materials two processes are commonly used: Cladding of an AgCd alloy strip with fine silver followed by complete oxidation results in a strip material with a small depletion area in the center of it's thickness and a Ag backing suitable for easy attachment by brazing (sometimes called “Conventional Ag/CdO”). Using a technology that allows the partial oxidation of a dual-strip AgCd alloy material in a higher pressure pure oxygen atmosphere yields a composite Ag/CdO strip material that has besides a relatively fine CdO precipitation also a easily brazable AgCd alloy backing (Fig. 2.85). These materials (DODURIT CdO ZH) are mainly used as the basis for contact profiles and contact tips.
During powder metallurgical production the powder mixed made by different processes are typically converted by pressing, sintering and extrusion to wires and strips. The high degree of deformation during hot extrusion produces a uniform and fine dispersion of CdO particles in the Ag matrix while at the same time achieving a high density which is advantageous for good contact properties (Fig. 2.84). To obtain a backing suitable for brazing, a fine silver layer is applied by either com-pound extrusion or hot cladding prior to or right after the extrusion (Fig. 2.86).
For larger contact tips, and especially those with a rounded shape, the single tip Press-Sinter-Repress process (PSR) offers economical advantages. The powder mix is pressed in a die close to the final desired shape, the “green” tips are sintered, and in most cases the repress process forms the final exact shape while at the same time increasing the contact density and hardness.
Using different silver powders and minor additives for the basic Ag and CdO starting materials can help influence certain contact properties for specialized applications.
Fig. 2.77: Strain hardening of internally oxidized Ag/CdO 90/10 by cold working
Fig. 2.78: Softening of internally oxidized Ag/CdO 90/10 after annealing for 1 hr after 40% cold working
Table 2.25: Physical and Mechanical Properties as well as Manufacturing Processes and Forms of Supply of Extruded Silver Cadmium Oxide (DODURIT CdO) Contact Materials
Fig. 2.79: Strain hardening of Ag/CdO 90/10 P by cold working
Fig. 2.80: Softening of Ag/CdO 90/10 P after annealing for 1 hr after 40% cold working
Fig. 2.81: Strain hardening of Ag/CdO 88/12 WP
Fig. 2.82: Softening of Ag/CdO 88/12WP after annealing for 1 hr after different degrees of cold working
Fig. 2.83: Micro structure of Ag/CdO 90/10 i.o. a) close to surface b) in center area
Fig. 2.84: Micro structure of Ag/CdO 90/10 P: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.85: Micro structure of Ag/CdO 90/10 ZH: 1) Ag/CdO layer 2) AgCd backing layer
Fig. 2.86: Micro structure of AgCdO 88/12 WP: a) perpendicular to extrusion direction b) parallel to extrusion direction
- Silver–tin oxide(SISTADOX)materials
Over the past years, many Ag/CdO contact materials have been replaced by Ag/SnO2 based materials with 2-14 wt% SnO2 because of the toxicity of Cadmium. This changeover was further favored by the fact that Ag/SnO2 contacts quite often show improved contact and switching properties such as lower arc erosion, higher weld resistance, and a significant lower tendency towards material transfer in DC switching circuits (Table 2.30). Ag/SnO2 materials have been optimized for a broad range of applications by other metal oxide additives and modification in the manufacturing processes that result in different metallurgical, physical and electrical properties (Table 2.29).
Manufacturing of Ag/SnO2 by internal oxidation is possible in principle, but during heat treatment of alloys containing > 5 wt% of tin in oxygen, dense oxide layers formed on the surface of the material prohibit the further diffusion of oxygen into the bulk of the material. By adding Indium or Bismuth to the alloy the internal oxidation is possible and results in materials that typically are rather hard and brittle and may show somewhat elevated contact resistance and is limited to applications in relays. To make a ductile material with fine oxide dispersion (SISTADOX TOS F) (Fig. 2.114) it is necessary to use special process variations in oxidation and extrusion which lead to materials with improved properties in relays. Adding a brazable fine silver layer to such materials results in a semifinished material suitable for the manufacture as smaller weld profiles (SISTADOX WTOS F) (Fig. 2.116). Because of their resistance to material transfer and low arc erosion these materials find for example a broader application in automotive relays (Table 2.31).
Powder metallurgy plays a significant role in the manufacturing of Ag/SnO2 contact materials. Besides SnO2 a smaller amount (<1 wt%) of one or more other metal oxides such as WO3, MoO3, CuO and/or Bi2O3 are added. These additives improve the wettability of the oxide particles and increase the viscosity of the Ag melt. They also provide additional benefits to the mechanical and arcing contact properties of materials in this group (Table 2.26).
In the manufacture the initial powder mixes different processes are applied which provide specific advantages of the resulting materials in respect to their contact properties (Figs. 2.87 – 2.119). Some of them are described here as follows:
- a) Powder blending from single component powders
In this common process all components including additives that are part of the powder mix are blended as single powders. The blending is usually performed in the dry stage in blenders of different design.
- b) Powder blending on the basis of doped powders
For incorporation of additive oxides in the SnO2 powder the reactive spray process (RSV) has shown advantages. This process starts with a waterbased solution of the tin and other metal compounds. This solution is nebulized under high pressure and temperature in a reactor chamber. Through the rapid evaporation of the water each small droplet is converted into a salt crystal and from there by oxidation into a tin oxide particle in which the additive metals are distributed evenly as oxides. The so created doped AgSnO2 powder is then mechanically mixed with silver powder.
- c) Powder blending based on coated oxide powders
In this process tin oxide powder is blended with lower meting additive oxides such as for example Ag2 MoO4 and then heat treated. The SnO2 particles are coated in this step with a thin layer of the additive oxide.
- d) Powder blending based on internally oxidized alloy powders
A combination of powder metallurgy and internal oxidation this process starts with atomized Ag alloy powder which is subsequently oxidized in pure oxygen. During this process the Sn and other metal components are transformed to metal oxide and precipitated inside the silver matrix of each powder particle.
- e) Powder blending based on chemically precipitated compound powders
A silver salt solution is added to a suspension of for example SnO2 together with a precipitation agent. In a chemical reaction silver and silver oxide respectively are precipitated around the additive metal oxide particles who act as crystallization sites. Further chemical treatment then reduces the silver oxide with the resulting precipitated powder being a mix of Ag and SnO2.
Further processing of these differently produced powders follows the conventional processes of pressing, sintering and hot extrusion to wires and strips. From these contact parts such as contact rivets and tips are manufactured. To obtain a brazable backing the same processes as used for Ag/CdO are applied. As for Ag/CdO, larger contact tips can also be manufactured more economically using the press-sinter-repress (PSR) process (Table 2.27).
Fig. 2.87: Strain hardening of Ag/SnO2 92/8 PE by cold working
Fig. 2.88: Softening of Ag/SnO2 92/8 PE after annealing for 1 hr after 40% cold working
Table 2.26: Physical and Mechanical Properties as well as Manufacturing Processes and Forms of Supply of Extruded Silver-Tin Oxide (SISTADOX) Contact Materials
Fig. 2.89: Strain hardening of Ag/SnO2 88/12 PE by cold working
Fig. 2.90: Softening of Ag/SnO2 88/12 PE after annealing for 1 hr after 40% cold working
Fig. 2.91: Strain hardening of oxidized Ag/SnO2 88/12 PW4 by cold working
Fig. 2.92: Softening of Ag/SnO2 88/12 PW4 after annealing for 1 hr after 30% cold working
Fig. 2.93: Strain hardening of Ag/SnO2 98/2 PX by cold working
Fig. 2.94: Softening of Ag/SnO2 98/2 PX after annealing for 1 hr after 80% cold working
Fig 2.95: Strain hardening of Ag/SnO2 92/8 PX by cold working
Fig. 2.96: Softening of Ag/SnO2 92/8 PX after annealing for 1 hr after 40% cold working
Fig. 2.97: Strain hardening of internally oxidized Ag/SnO2 88/12 TOS F by cold working
Fig. 2.98: Softening of Ag/SnO2 88/12 TOS F after annealing for 1 hr after 30% cold working
Fig. 2.99: Strain hardening of internally oxidized Ag/SnO2 88/12P by cold working
Fig. 2.100: Softening of Ag/SnO2 88/12P after annealing for 1 hr after 40% cold working
Fig. 2.101: Strain hardening of Ag/SnO2 88/12 WPC by cold working
Fig. 2.102: Softening of Ag/SnO2 88/12 WPC after annealing for 1 hr after different degrees of cold working
Fig. 2.103: Strain hardening of Ag/SnO2 86/14 WPC by cold working
Fig. 2.104: Softening of Ag/SnO2 86/14 WPC after annealing for 1 hr after different degrees of cold working
Fig. 2.105: Strain hardening of Ag/SnO2 88/12 WPD by cold working
Fig. 2.106: Softening of Ag/SnO2 88/12 WPD after annealing for 1 hr after different degrees of cold working
Fig. 2.108: Softening of Ag/SnO2 88/12 WPX after annealing for 1 hr after different degrees of cold working
Fig. 2.107: Strain hardening of Ag/SnO2 88/12 WPX by cold working
Fig. 2.109: Micro structure of Ag/SnO2 92/8 PE: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.110: Micro structure of Ag/SnO2 88/12 PE: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.111: Micro structure of Ag/SnO2 88/12 PW: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.112: Micro structure of Ag/SnO2 98/2 PX: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.113: Micro structure of Ag/SnO2 92/8 PX: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.114: Micro structure of Ag/SnO2 88/12 TOS F: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.115: Micro structure of Ag/SnO2 86/14 WPC: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) AgSnO2 contact layer, 2) Ag backing layer
Fig. 2.116: Micro structure of Ag/SnO2 92/8 WTOS F: a) perpendicular to extrusion direction b) parallel to extrusion direction,1) AgSnO2 contact layer, 2) Ag backing layer
Fig. 2.117: Micro structure of Ag/SnO2 88/12 WPD: parallel to extrusion direction 1) AgSnO2 contact layer, 2) Ag backing layer
Fig. 2.118: Micro structure of Ag/SnO2 88/12 WPX:parallel to extrusion direction 1) AgSnO2 contact layer, 2) Ag backing layer
Fig. 2.119: Micro structure of Ag/SnO2 86/14 WPX: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) AgSnO2 contact layer, 2) Ag backing layer
Table 2.27: Physical Properties of Powder Metallurgical Silver-Metal Oxide Materials with Fine Silver Backing Produced by the Press-Sinter-Repress Process
- Silver–zinc oxide (DODURIT ZnO) materials
Silver zinc oxide (DODURIT ZnO) contact materials with mostly 6 - 10 wt% oxide content including other small metal oxides are produced exclusively by powder metallurgy (Figs. 2.120 – 2.125) (Table 2.28). Adding Ag2WO4 in the process b) as described in the preceding chapter on Ag/SnO2 has proven most effective for applications in AC relays, wiring devices, and appliance controls. Just like with the other Ag metal oxide materials, semi-finished materials in strip and wire form are used to manufacture contact tips and rivets. Because of their high resistance against welding and arc erosion Ag/ZnO materials present an economic alternative to Cd free Ag-tin oxide contact materials (Tables 2.30 and 2.31).
Table 2.28: Physical and Mechanical Properties as well as Manufacturing Processes and Forms of Supply of Extruded Silver-Zinc Oxide (DODURIT ZnO) Contact
Fig. 2.120: Strain hardening of Ag/ZnO 92/8 PW25 by cold working
Fig. 2.121: Softening of Ag/ZnO 92/8 PW25 after annealing for 1 hr after 30% cold working
Fig. 2.122: Strain hardening of Ag/ZnO 92/8 WPW25 by cold working
Fig. 2.123: Softening of Ag/ZnO 92/8 WPW25 after annealing for 1hr after different degrees of cold working
Fig. 2.115: Micro structure of Ag/ZnO 92/8 Pw25: a) perpendicular to extrusion direction b) parallel to extrusion direction
Fig. 2.116: Micro structure of Ag/ZnO 92/8 WPW25:a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) Ag/ZnO contact layer, 2) Ag backing layer
Table 2.29: Optimizing of Silver–Tin Oxide Materials Regarding their Switching Properties and Forming Behavior
Table 2.30: Contact and Switching Properties of Silver–Metal Oxide Materials
Table 2.31: Application Examples of Silver–Metal Oxide Materials
Silver–Graphite (GRAPHOR)-Materials
Ag/C (GRAPHOR) contact materials are usually produced by powder metallurgy with graphite contents of 2 – 5 wt% (Table 2.32). The earlier typical manufacturing process of single pressed tips by pressing - sintering - repressing (PSR) has been replaced in Europe for quite some time by extrusion. In North America and some other regions however the PSR process is still used to some extend mainly for cost reasons.
The extrusion of sintered billets is now the dominant manufacturing method for semi-finished AgC materials (Figs. 2.126 – 2.129). The hot extrusion process results in a high density material with graphite particles stretched and oriented in the extrusion direction (Figs. 2.130 – 2.133). Depending on the extrusion method in either rod or strip form the graphite particles can be oriented in the finished contact tips perpendicular (GRAPHOR) or parallel (GRAPHOR D) to the switching contact surface (Figs. 2.131 and 2.132).
Since the graphite particles in the Ag matrix of Ag/C materials prevent contact tips from directly being welded or brazed, a graphite free bottom layer is required. This is achieved by either burning out (de-graphitizing) the graphite selectively on one side of the tips or by compound extrusion of a Ag/C billet covered with a fine silver shell.
Ag/C contact materials exhibit on the one hand an extremely high resistance to contact welding but on the other have a low arc erosion resistance. This is caused by the reaction of graphite with the oxygen in the surrounding atmosphere at the high temperatures created by the arcing. The weld resistance is especially high for materials with the graphite particle orientation parallel to the arcing contact surface. Since the contact surface after arcing consists of pure silver the contact resistance stays consistently low during the electrical life of the contact parts.
A disadvantage of the Ag/C materials is their rather high erosion rate. In materials with parallel graphite orientation this can be improved if part of the graphite is incorporated into the material in the form of fibers (GRAPHOR DF), (Fig. 2.133). The weld resistance is determined by the total content of graphite particles.
Ag/C tips with vertical graphite particle orientation are produced in a specific sequence: Extrusion to rods, cutting of double thickness tips, burning out of graphite to a controlled layer thickness, and a second cutting to single tips. Such contact tips are especially well suited for applications which require both, a high weld resistance and a sufficiently high arc erosion resistance (Table 2.33). For attachment of Ag/C tips welding and brazing techniques are applied.
welding the actual process depends on the material's graphite orientation. For Ag/C tips with vertical graphite orientation the contacts are assembled with single tips. For parallel orientation a more economical attachment starting with contact material in strip or profile tape form is used in integrated stamping and welding operations with the tape fed into the weld station, cut off to tip form and then welded to the carrier material before forming the final contact assembly part. For special low energy welding the Ag/C profile tapes GRAPHOR D and DF can be pre-coated with a thin layer of high temperature brazing alloys such as CuAgP.
In a rather limited way, Ag/C with 2 – 3 wt% graphite can be produced in wire form and headed into contact rivet shape with low head deformation ratios.
The main applications for Ag/C materials are protective switching devices such as miniature molded case circuit breakers, motor-protective circuit breakers, and fault current circuit breakers, where during short circuit failures highest resistance against welding is required (Table 2.34). For higher currents the low arc erosion resistance of Ag/C is compensated by asymmetrical pairing with more erosion resistant materials such as Ag/Ni and Ag/W.
Fig. 2.126: Strain hardening of Ag/C 96/4 D by cold working
Fig. 2.127: Softening of Ag/C 96/4 D after annealing
Fig. 2.128: Strain hardening of Ag/C DF by cold working
Fig. 2.129: Softening of Ag/C DF after annealing
Fig. 2.130: Micro structure of Ag/C 97/3: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) Ag/C contact layer, 2) Ag backing layer
Fig. 2.131: Micro structure of Ag/C 95/5: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) Ag/C contact layer, 2) Ag backing layer
Fig. 2.132: Micro structure of Ag/C 96/4 D: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) Ag/C contact layer, 2) Ag backing layer
Fig. 2.133: Micro structure of Ag/C DF: a) perpendicular to extrusion direction b) parallel to extrusion direction, 1) Ag/C contact layer, 2) Ag/Ni 90/10 backing layer
Table 2.32: Physical Properties of Silver–Graphite (GRAPHOR) Contact Materials
Table 2.33: Contact and Switching properties of Silver–Graphite (GRAPHOR) Contact Materials
Table 2.34: Application Examples and Forms of Supply of Silver– Graphite (GRAPHOR) Contact Materials
Pre-Production of Contact Materials (Bild)
Tungsten and Molybdenum Based Materials
Tungsten and Molybdenum (Pure Metals)
Tungsten is characterized by its advantageous properties of high melting and boiling points, sufficient electrical and thermal conductivity and high hardness and density (Table 2.35). It is mainly used in the form of brazed contact tips for switching duties that require a rapid switching sequence such as horn contacts for cars and trucks.
Molybdenum has a much lesser importance as a contact material since it is less resistant against oxidation than tungsten. Both metals are however used in large amounts as components in composite materials with silver and copper.
Table 2.35: Mechanical Properties of Tungsten and Molybdenum
Silver–Tungsten (SIWODUR) Materials
Ag/W (SIWODUR) contact materials combine the high electrical and thermal conductivity of silver with the high arc erosion resistance of the high melting tungsten metal (Table 2.36). The manufacturing of materials with typically 50-80 wt% tungsten is performed by the powder metallurgical processes of liquid phase sintering or by infiltration. Particle size and shape of the starting powders are determining the micro structure and the contact specific properties of this material group (Figs. 2.134 and 2.135) (Table 2.37).
During repeated switching under arcing loads tungsten oxides and mixed oxides (silver tungstates – Ag2 WO4 ) are formed on the Ag/W surface creating 2 4 poorly conducting layers which increase the contact resistance and by this the temperature rise during current carrying. Because of this fact the Ag/W is paired in many applications with Ag/C contact parts.
Silver–tungsten contact tips are used in a variety of shapes and are produced for the ease of attachment with a fine silver backing layer and quite often an additional thin layer of a brazing alloy. The attachment to contact carriers is usually done by brazing, but also by direct resistance welding for smaller tips.
Ag/W materials are mostly used as the arcing contacts in disconnect switches for higher loads and as the main contacts in small and medium duty power switches and industrial circuit breakers (Table 2.38). In north and south america they are also used in large volumes in miniature circuit breakers of small to medium current ratings in domestic wiring as well as for commercial power distribution.
Silver–Tungsten Carbide (SIWODUR C) Materials
This group of contact materials contains the typically 40-65 wt-% of the very hard and erosion wear resistant tungsten carbide and the high conductivity silver (Fig. 2.135) (Table 2.36). Compared to Ag/W the Ag/WC (SIWODUR C) materials exhibit a higher resistance against contact welding (Table 2.37). The rise in contact resistance experienced with Ag/W is less pronounced in Ag/WC because during arcing a protective gas layer of CO is formed which limits the reaction of oxygen on the contact surface and therefore the formation of metal oxides.
Higher requirements on low temperature rise can be fulfilled by adding a small amount of graphite which however increases the arc erosion. Silver–tungsten carbide–graphite materials with for example 27 wt% WC and 3 wt% graphite or 16 wt% WC and 2 wt% graphite are manufactured using the single tip press-sinter-repress (PSR) process (Fig. 2.136).
The applications of Ag/WC contacts are similar to those for Ag/W (Table 2.38).
Silver–Molybdenum (SILMODUR) Materials
Ag/Mo materials with typically 50-70 wt% molybdenum are usually produced by the powder metallurgical infiltration process (Fig. 2.137) (Table 2.36). Their contact properties are similar to those of Ag/W materials (Table 2.37). Since the molybdenum oxide is thermally less stable than tungsten oxide the self-cleaning effect of Ag/Mo contact surface during arcing is more pronounced and the contact resistance remains lower than that of Ag/W. The arc erosion resistance of Ag/Mo however is lower than the one for Ag/W materials. The main applications for Ag/Mo contacts are in equipment protecting switching devices (Table 2.38).
Fig. 2.134: Micro structure of Ag/W 25/75
Fig. 2.135: Micro structure of Ag/WC 50/50
Fig. 2.136: Micro structure of Ag/WC27/C3
Fig. 2.137: Micro structure of Ag/Mo 35/65
Table 2.36: Physical Properties of Contact Materials Based on Silver–Tungsten (SIWODUR), Silver–Tungsten Carbide (SIWODUR C) and Silver Molybdenum (SILMODUR)
Table 2.37: Contact and Switching Properties of Contact Materials Based on Silver – Tungsten (SIWODUR), Silver–Tungsten Carbide (SIWODUR C) and Silver Molybdenum (SILMODUR)
Table 2.38: Application Examples and Forms of Supply for Contact Materials Based on Silver–Tungsten (SIWODUR), Silver–Tungsten Carbide (SIWODUR C) and Silver Molybdenum (SILMODUR)
Copper–Tungsten (CUWODUR) Materials
Copper–tungsten (CUWODUR) materials with typically 50-85 wt% tungsten are produced by the infiltration process with the tungsten particle size selected according to the end application (Figs. 2.138 – 2.141) (Table 2.39). To increase the wettability of the tungsten skeleton by copper a small amount of nickel < 1 wt% is added to the starting powder mix.
W/Cu materials exhibit a very high arc erosion resistance (Table 2.40). Compared to silver–tungsten materials they are however less suitable to carry permanent current.
With a solid tungsten skeleton as it is the case for W/C infiltrated materials with 70-85 wt% tungsten the lower melting component copper melts and vaporizes in the intense electrical arc. At the boiling point of copper (2567°C) the still solid tungsten is efficiently “cooled” and remains pretty much unchanged.
During very high thermal stress on the W/Cu contacts, for example during short circuit currents > 40 kA the tungsten skeleton requires special high mechanical strength. For such applications a high temperature sintering of tungsten from selected particle size powder is applied before the usual infiltration with copper (example: CUWODUR H).
For high voltage load switches the most advantageous contact system consists of a contact tulip and a contact rod. Both contact assemblies are made usually from the mechanically strong and high conductive CuCrZr material and W/Cu as the arcing tips. The thermally and mechanically highly stressed attachment between the two components is often achieved by utilizing electron beam welding or capacitor discharge percussion welding. Other attachment methods include brazing and cast-on of copper followed by cold forming steps to increase hardness and strength.
The main application areas for CUWODUR materials are as arcing contacts in load and high power switching in medium and high voltage switchgear as well as electrodes for spark gaps and over voltage arresters (Table 2.41).
Table 2.39: Physical Properties of Copper–Tungsten (CUWODUR) Contact Materials
Fig. 2.139: Micro structure of W/Cu 70/30 G Fig. 2.140: Micro structure of W/Cu 70/30 H
Fig. 2.138: Micro structure of W/Cu 70/30 F Fig. 2.141: Micro structure of W/Cu 80/20 H
Manufacturing of Contact Parts for Medium and High Voltage Switchgear
Table 2.40: Contact and Switching Properties of Copper–Tungsten (CUWODUR) Contact Materials
Table 2.41: Application Examples and Forms of Supply for Tungsten– Copper (CUWODUR) Contact Materials
Special Contact Materials (VAKURIT) for Vacuum Switches
The trade name VAKURIT is assigned to a family of low gas content contact materials developed for the use in vacuum switching devices (Table 2.42).
Low Gas Content Materials Based on Refractory Metals
Contact materials of W/Cu, W/Ag, WC/Ag, or Mo/Cu can be used in vacuum switches if their total gas content does not exceed approximately 150 ppm. In the low gas content W/Cu (VAKURIT) material mostly used in vacuum contactors the high melting W skeleton is responsible for the high erosion resistance when combined with the high conductivity copper component which evaporates already in noticeable amounts at temperatures around 2000 °C.
Since there is almost no solubility of tungsten, tungsten carbide, or molybdenum in copper or silver the manufacturing of these material is performed powdermetallurgically. The W, WC, or Mo powders are pressed and sintered and then infiltrated with low gas content Cu or Ag. The content of the refractory metals is typically between 60 and 85 wt% (Figs. 2.142 and 2.143).
By adding approximately 1 wt% antimony the chopping current, i.e. the abrupt current decline shortly before the natural current-zero, can be improved for W/Cu (VAKURIT) materials (Table 2.43). The contact components mostly used in vacuum contactors are usually shaped as round discs. These are then attached by brazing in a vacuum environment to their contact carriers (Table 2.44).
Low Gas Content Materials Based on Copper-Chromium
As contact materials in vacuum interupters in medium voltage devices low gas materials based on Cu/Cr have gained broad acceptance. The typical chromium contents are between 25 and 55 wt% (Figs. 2.144 and 2.145). During the powder metallurgical manufacturing a mix of chromium and copper powders is pressed into discs and subsequently sintering in a reducing atmosphere or vacuum below the melting point of copper. This step is followed by cold or hot re-pressing. Depending on the composition the Cu/Cr (VAKURIT) materials combine a relatively high electrical and thermal conductivity with high dielectric stability. They exhibit a low arc erosion rate and good resistance against welding as well as favorable values of the chopping current in medium voltage load switches, caused by the combined effects of the two components, copper and chromium (Table 2.43).
The switching properties of Cu/Cr (VAKURIT) materials are dependent on the purity of the Cr metal powders and especially the type and quantity of impurities contained in the chromium powder used. Besides this the particle size and distribution of the Cr powder are of high importance. Because of the getter activity of chromium a higher total gas content of up to about 650 ppm compared to the limits in refractory based materials can be tolerated in these Cu/Cr contact materials. Besides the more economical sinter technology also infiltration and vacuum arc melting are used to manufacture these materials. Cu/Cr contacts are supplied in the shape of discs or rings which often also contain slots especially for vacuum load switches in medium voltage devices (Table 2.44). Increased applications of round discs can also be observed for low voltage vacuum contactors.
Table 2.42: Physical Properties of the Low Gas Materials (VAKURIT) for Vacuum Switches
Fig. 2.142: Micro structure of W/Cu 30Sb1 – low gas
Fig. 2.143: Micro structure of WC/Ag 50/50 – low gas
Fig. 2.144: Micro structure of Cu/Cr 75/25 – low gas
Fig. 2.145: Micro structure of Cu/Cr 50/50 – low gas
Table 2.43: Contact and Switching Properties of VAKURIT Materials
Table 2.44: Application Examples and Form of Supply for VAKURIT Materials
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Manufacturing Equipment for Semi-Finished Materials (Bild)