Capacitor-grade lead wires with increased tensile strength and hardness

Information

  • Patent Grant
  • 7056470
  • Patent Number
    7,056,470
  • Date Filed
    Tuesday, January 21, 2003
    21 years ago
  • Date Issued
    Tuesday, June 6, 2006
    18 years ago
Abstract
A capacitor-grade wire made from powder metallurgy containing at least niobium and silicon, wherein the niobium is the highest weight percent metal present in the niobium wire. The wire having a controlled tensile strength at finish diameter exceeds the strength of capacitor-grade wire formed by ingot metallurgy. Also, the powder metallurgy wire hardness exceeds capacitor-grade wire formed from ingot metallurgy with electrical leakage meeting the specifications normally applied to capacitor grade tantalum, niobium or niobium-zirconium lead wire at sinter temperatures of about 1150° C. and above.
Description
FIELD OF THE INVENTION

The invention relates generally to capacitor lead wires, more particularly to niobium lead wires usable with anode compacts of tantalum or niobium. The invention includes niobium powder metallurgy derived lead wires of niobium doped with silicon, preferably having improved strength and hardness without significant detriment to electrical leakage rating of the wire.


BACKGROUND OF THE INVENTION

Niobium and niobium alloy lead wires with melt source derivation have been used as capacitor lead wires. Pure niobium wires of melt process origin have low electrical leakage at sintering temperatures of 1150° C. and above. However the wires are limited in tensile strength and hardness, which make them difficult to work with; this results in low production through put when bonding the wires to the capacitor anode compacts and/or in the course of sintering the compact or prolysis of solid electrolyte with the lead wire attached. Niobium alloys, such as niobium-zirconium have better tensile strength then pure niobium wires of melt process origin and acceptable electrical leakage above 1150° C. However above 1050° C. zirconium diffuses off the wire and contaminates the anode, making it unacceptable as a capacitor lead wire.


SUMMARY OF THE INVENTION

It is an object of the present invention to improve chemical, mechanical, metallurgical, and functional consistency of capacitor grade lead wires.


It is a further object of the present invention to reduce sintering and bonding problems.


It is yet a further object of the present invention to improve niobium wire to overcome the above-described disadvantages without significantly impacting the electrical properties of the wire and wire-anode assembly.


The invention relates to a process for making a capacitor grade silicone-doped niobium lead wire comprising (a) forming a low oxygen niobium powder by hydriding a niobium ingot or a niobium bar and grinding or milling the ingot or the bar, and thereby making a powder having a Fisher Average Particle Diameter particle size range of less than about 150 microns, (b) dehyriding the powder, and optionally deoxidizing the powder, forming a low oxygen niobium powder, (c) blending the low oxygen niobium powder with a silicon additive powder and compacting the powder by cold isostatic pressing to a bar; (d) thermomechanically processing the bar into a rod, and (e) subjecting the rod to a combination of rolling and cold drawning steps, and forming the silicon doped wire. The invention also relates to a method made from such a process.


The present invention includes a niobium wire made from powder metallurgy (P/M), containing a silicon additive of less than about 600 ppm. Generally, the amount of silicon ranges from about 150 to about 600 ppm. Preferably, the amount of silicon ranges from about 150 to 300 ppm. The invention imparts a controlled, higher mechanical tensile strength in the niobium wire at finish diameter that exceeds capacitor-grade wire formed from niobium and niobium-zirconium alloys derived directly from ingot metallurgy (I/M). Preferably too the P/M source niobium has oxygen content below 400 ppm, even when silicon is added in an oxide form. The P/M derived niobium, and niobium-silicon wires also have increased hardness that exceeds hardness of capacitor-grade wire of I/M niobium and niobium-zirconium wires and electrical leakage within current specifications at sinter temperatures of about 1150° C. and above, or about 1250 and above. The P/M source material if sintered at well below about 1150° C. or 1250° C. and above, and/or attached to anode compacts sintered below about 1150° C. or below 1250° C. would have higher leakage. But at about 1150° C. or 1250° C. and above, the differences become minimal.


It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are intended to provide further explanation of the present invention as described.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a chart of the ultimate tensile strength as a function of wire diameter of select niobium and niobium alloy wire of the present invention derived from powder metallurgy compared to niobium and niobium alloy wire derived from ingot metallurgy;



FIG. 2 is a chart of electrical DC leakage as a function of sintering temperature of select niobium and niobium alloy wire of the present invention derived from powder metallurgy compared to niobium and niobium alloy wire derived from ingot metallurgy;



FIG. 3A-3F are side and front views of examples of capacitor lead wires bonded to anode compacts; and



FIG. 4 is a chart of electrical DC leakage as a function of sintering temperature of select niobium and niobium alloy wire of the present invention derived from powder metallurgy compared to niobium and niobium alloy wire derived from ingot metallurgy.





DETAILED DESCRIPTION OF THE INVENTION

One of the preferred embodiments of the invention is a lead wire of silicone-doped niobium made as follows. Niobium powders are formed by hydriding an ingot or bar of niobium and grinding or otherwise milling the ingot or bar to create a powder at a size range of less than 150 microns FAPD (Fisher Average Particle Diameter), dehyriding and deoxidating. The hydride-grind process as disclosed in U.S. Pat. No. 3,295,951 of Fincham et al and the deoxidation (with a combined dehydriding deoxidation) is described in U.S. Pat. No. 6,261,337 of Kumar, incorporated herein by reference in their entirety, both said patents are of common assignment with this application and Mr. Kumar as a joint inventor of the present invention. The niobium powder preferably is attained with an oxygen level below 400 ppm, preferably below 200 ppm. A silicon additive powder is blended with the low oxygen niobium powder, compacted by cold isostatic pressing (at up to 60 KSI) to a preform billet for extrusion or sinter bar preferably yeilding a bar approximately 1.3 inches diameter. The bar is thermomechanically processed to a rod. The rod is then rolled (or swaged) and cold drawn, typically with a schedule of reductions and intermediate anneals as follows:


Annealed at 2500° F. for 1.5 hours;


Rolled to 0.440 inches diameter;


Annealed at 2500° F. for 1.5 hours;


Reduced to 0.103 inches diameter;


Drawn to 0.0346 inches diameter wire;


Drawn to a finish diameter.


Stated in general terms, the rod can be rolled (or swaged) and cold drawn, typically with a schedule of reductions and intermediate anneals as follows:


Annealed at a temperature ranging from about 2100° F. to about 2700° F. for a time ranging from about 0.5 hours to about 2.0 hours;


Rolled from a diameter ranging from about 1 inch to about 0.25 inches diameter;


Annealed at a temperature ranging from about 2100 to about 2700° F. for a time ranging from about 0.5 hours to about 2.0 hours;


Reduced from about 1 inch to about to 0.075 inches diameter;


Drawn to a finish diameter.


The diameter of the wire made in accordance to the invention can range from about 0.005 inches to about 0.1 inches. The wire of the present invention can contain other additional ingredients such as other metals or ingredients typically added to niobium metal, such as tantalum, zirconium, titanium, or mixtures thereof. The types and amounts of these additional ingredients can be the same as those used with conventional niobium and would be known to those skilled in the art. TABLE 1 below lists the chemistry of the specimens used in certain Experiments 1–5 of silicon doped niobium wire of powder metallurgy origin as reduced to 0.5 inch diameter and 0.103 inch diameter.

























TABLE 1





PPM

C
O
N
Mg
Al
Si
Ti
Cr
Fe
Ni
Cu
Zr
Mo
Ta
W































Experiment #1
½″
88
646
47
114
20
25
20
108
655
157
10
10
20
1388
200


Experiment #2
½″
90
301
42
106
20
158
20
99
574
133
16
10
20
8374
200


Experiment #3
½″
54
322
60
120
0.5
13
6.1
45
225
44
4
5
1
3000
5


Experiment #4
½″
142
358
60
120
1.1
161
5.3
50
255
53
3.5
5
1
10000
7.1


Experiment #5
½″
58
329
72
95
2.7
306
5.5
45
230
53
7
5
1
20000
7.5


Experiment #1
.103″
63
173
31
110
2
23
2
140
500
130
4
5
11
1000
55


Experiment #2
.103″
71
180
28
105
3
163
2
150
675
150
6.4
5
11
10000
85


Experiment #3
.103″
57
262
49
85
5.2
12
7.5
65
100
55
1.9
5
1
5000
6.8


Experiment #4
.103″
79
291
52
100
4.1
162
6.1
63
130
65
2.2
5
1
10000
5.7


Experiment #5
.103″
61
282
59
80
2.8
294
4.9
63
70
55
1.9
5
1
10000
6.5









Wires were prepared from the silicon master blends presented in Experiments 1–5 of TABLE 1, and sample were taken at various size milestones and tested for tensile strength and hardness (Rockwell hardness B scale, HRB). I/M derived niobium-zirconium wires (prior art) were also tested similarly.





















TABLE 2






Prior Art

Nb PM

Nb PM

Nb PM

Nb PM

Nb PM




NbZr

Exp. #1

Exp. #2

Exp. #3

Exp. #4

Exp. #5



Ingot

(25 ppm)

(150 ppm)

(10 ppm)

(150 ppm)

(300 ppm)


Size
Hardness
Tensil
Hardness
Tensil
Hardness
Tensil
Hardness
Tensil
Hardness
Tensil
Hardness
Tensil


In
HRB
KSI
HRB
KSI
HRB
KSI
HRB
KSI
HRB
KSI
HRB
KSI



























0.6
83.7

73

74.3

75.7

76.5

80.2



0.42
82.4

74.9

73.2

36.7

39.7

43.1



0.266
89.8

74.4

71

74.3

76.9

79.1



0.166
89.1

74.5

76.6

79.9

81

81.1



0.107
87.7

72

81

82

82.5

84.7



0.103
79.2

85.6

86.1

84.4

86.4

87.5



0.0933
68.5
41
80.8
53
76.9
55.6


0.0845
72.3
47
78.7
57.1
79.5
58.32


0.0765
71.6
47.2
81.4
59.72
82.7
62.5


0.0693
72.7
52.8
83.4
62.12
82.4
64.86


0.0627
75.4
55
82.4
68.3
83.7
69.9


0.0568
75.4
55.9
85
72.53
84.3
75.1


0.0514
76.9
62.5
83.7
75.6
85.4
77.7
89
119.88
91.5
122.28
98
125.94


0.0465
77.2
64.4
84
76.1
86.3
78.7
87
124.65
90.5
130.17
96.8
132.48


0.0422
78.3
66.7
85.4
81.28
84.7
82.7
92.5
126.05
91.7
133.49
97.4
132.83


0.0382
79
65.5
86.5
83.5
85.8
84.2
88.3
131.23
93.2
138.43
97.6
137.2


0.0344
85
70.31
88.5
89
85.6
87.7
90
130.57
92.5
143.76
97.5
139.88


0.02878
83.7
71.22
86.5
93.8
87.1
94.6
93
133.74
94.2
142.57
99.6
141.34


0.02634
84.7
72.21
88.5
95.2
88.5
96.3
96.7
150.2
99.7
154.8
99.7
174.64


0.02431
85
72.93
89
101
89.5
99.7
96.4
168.63
98
180.61
98.1
182.2


0.0223
87.3
74.63
89
99.3
89.9
103.3
99.3
178.14
99.4
180.66
100.3
182.4


0.02062
87.6
75.88
90.5
103.4
91.4
106.8
98.8
188.97
100.2
206.86
99.7
192.47


0.01995
87.8
83.56
90.7
112.32
90.7
114.98
99.7
164.45
100.2
172.85
102
158.6


0.0173
85
82.30
90.1
116.8
90.5
117.66
100.5
168.54
101.5
179.12
101.6
166.84


0.01537
86.8
73.36
91
119.56
91.2
121
99.7
172.73
103.6
182.28
102.2
172.94


0.01334
87.8
73.36
90.6
126.95
91
128.43
100
176.76
104.6
187.1
102.2
179.5









As can be seen from the results in TABLE 2 and FIG. 1, the niobium-silicon wire had a much higher tensile strength and hardness than the niobium-zirconium wire at about 0.050 inches diameter and below.


Also, electrical leakage tests (40 volts at 90%) were conducted for wire (wire-anode assemblies in capacitor test conditions) or anodes with select silicon master blends (Experiments #1 and #2) and presented in FIG. 2. The tests were conducted for anode assemblies with lead wires made at various sintering temperatures. As can be seen from the results in TABLE 3 below and FIG. 2, the niobium-silicon wire is acceptable for use at sintering temperatures of 1250° C. and above, but not lower, complying with the current tantalum capacitor grade wire specification leakage of 0.6 μA/in2 at 1250° C.











TABLE 3







(@1250° C.)



Leakage



μA/in2



















niobium ingot
0.1



niobium-zirconium
0.25



Experiment #1
0.35



Experiment #2
0.6



Specification
0.6










Side and front views of examples of niobium-silicon capacitor lead wires of the present invention bonded to anode compacts are illustrated in FIGS. 3A–3F. FIGS. 3A and 3B illustrate a niobium-silicon capacitor lead wire 10 butt welded to an anode compact 12. FIGS. 3C and 3D illustrate a niobium-silicon capacitor lead wire 10 imbedded for a length 14 within compact 12. FIGS. 3E and 3F illustrated yet another attachment technique of welding the lead wire 10 to the top 16 of the compact 12. The lead wire 10 of any of FIGS. 3A–3F and/or the compact 12 of any such figures can be circular or flat (ribbon form) or other shapes.


Also, electrical leakage tests (40 volts at 90%) were conducted for wire (wire-anode assemblies in capacitor test conditions) or anodes with select silicon master blends (Experiments #3, 4 and 5) and presented in FIG. 4. The tests were conducted for anode assemblies with lead wires made at various sintering temperatures. As can be seen from the results in TABLE 4 below and FIG. 4, the niobium-silicon wire is acceptable for use at sintering temperatures of 1150° C. and above, but not lower, complying with the current tantalum capacitor grade wire specification leakage of 0.6 μA/in2 at 1150° C.











TABLE 4







(@1150° C.)



Leakage



μA/in2



















niobium ingot
0.1



niobium-zirconium
0.25



Experiment #3
0.09



Experiment #4
0.118



Experiment #5
0.103



Specification
0.6










Artifacts of electrolyte impregnation and pyrolysis cathode attachment and packaging all well known to those skilled in the art are omitted from the figures for convenience of illustration


Other embodiments of the present invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only.

Claims
  • 1. A process for making a silicone-doped niobium lead wire comprising: (a) forming a low oxygen niobium powder by hydriding a niobium ingot or a niobium bar and grinding or milling the ingot or the bar, and thereby making a powder having a Fisher Average Particle Diameter particle size range of less than 150 microns;(b) (i) dehydriding the niobium powder, and (ii) deoxidating the dehydrided niobium powder thereby forming a low oxygen niobium powder;(c) blending the low oxygen niobium powder with a silicon additive powder, and compacting the powder blend of low oxygen niobium powder and silicon additive powder by cold isotactic pressing to form a bar;(d) thermomechanically processing the bar into a rod; and(e) subjecting the rod to the following sequential steps, (i) annealing at a temperature of about 2500° F. for 1.5 hours,(ii) rolling to a diameter of about 0.440 inches,(iii) annealing at a temperature of about 2500° F. for 1.5 hours(iv) reducing to a diameter of about 0.1 inches, and(v) drawing to a wire having a diameter of at least about 0.005 inches.
  • 2. The process of claim 1, wherein the silicon is added in an amount that is less than about 600 ppm.
  • 3. The process of claim 1, wherein the silicon is added in an amount ranging from about 150 to about 300 ppm.
  • 4. The process of claim 1, wherein the wire further comprises a metal component selected from the group consisting of tantalum, zirconium, titanium, and combinations thereof.
  • 5. The process of claim 1, wherein the niobium powder has an oxygen level that is below about 400 ppm.
  • 6. The process of claim 1, wherein the wire has a tensile strength exceeding capacitor-grade niobium wire and niobium-zirconium alloys derived directly from ingot metallurgy.
  • 7. The process of claim 1 wherein the niobium powder has an oxygen level of less than 200 ppm.
Parent Case Info

This application is based on International Application No. PCT/US03/01822, filed Jan. 21, 2003, which was based on Provisional Application No. 60/351,554 filed Jan. 24, 2002.

PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/US03/01822 1/21/2003 WO 00 10/4/2004
Publishing Document Publishing Date Country Kind
WO2004/003949 1/8/2004 WO A
US Referenced Citations (16)
Number Name Date Kind
3295951 Fincham et al. Jan 1967 A
4084965 Fry Apr 1978 A
4235629 Marsh et al. Nov 1980 A
4441927 Getz et al. Apr 1984 A
4555268 Getz Nov 1985 A
5482672 Friedman et al. Jan 1996 A
6261337 Kumar Jul 2001 B1
6269536 Balliett Aug 2001 B1
6402066 Habecker et al. Jun 2002 B1
6521173 Kumar et al. Feb 2003 B1
6558447 Shekhter et al. May 2003 B1
6600646 Naito Jul 2003 B1
20030089197 Wada et al. May 2003 A1
20030218857 Omori et al. Nov 2003 A1
20040111849 Omori et al. Jun 2004 A1
20040244531 Sato et al. Dec 2004 A1
Foreign Referenced Citations (2)
Number Date Country
2 185 756 Jul 1987 GB
2185756 Jul 1987 GB
Related Publications (1)
Number Date Country
20050031481 A1 Feb 2005 US
Provisional Applications (1)
Number Date Country
60351554 Jan 2002 US