[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US3128178A - Tantalum-titanium base alloy - Google Patents

Tantalum-titanium base alloy Download PDF

Info

Publication number
US3128178A
US3128178A US92151A US9215161A US3128178A US 3128178 A US3128178 A US 3128178A US 92151 A US92151 A US 92151A US 9215161 A US9215161 A US 9215161A US 3128178 A US3128178 A US 3128178A
Authority
US
United States
Prior art keywords
tantalum
alloy
weight
hot
corrosion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US92151A
Inventor
Jr Edward F Duffek
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
California Research LLC
Original Assignee
California Research LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by California Research LLC filed Critical California Research LLC
Priority to US92151A priority Critical patent/US3128178A/en
Application granted granted Critical
Publication of US3128178A publication Critical patent/US3128178A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/02Alloys based on vanadium, niobium, or tantalum

Definitions

  • This invention relates to tantalum-titanium base metal alloys, particularly to such alloys which contain alloying metals of vanadium and nickel as essential components, which make the resulting alloys ductile and resistant to corrosion by hot oxidizing and hot non-oxidizing acids.
  • Alloys with the above properties are most useful for lining chemical reaction vessels, auxiliary equipment and connecting lines, which are exposed to hot phosphoric acid and hot sulfuric acid.
  • Liquid phosphoric acid is recognized as an efficient catalyst for certain organic chemical reactions, including alkylation and isomerization and the polymerization of normally gaseous olefins. Corrosive attack appears to be the greatest with aqueous solutions of about 85% phosphoric acid. While considerable progress has been made in controlling corrosion in the presence of liquid phosphoric acid (see, for example, Kemp and Zeh Patent 2,65 3,177 and Piehl Patent 2,854,- 497), there is need for further improvement and particularly for alloys which are also resistant to corrosion in the presence of hot oxidizing acids such as sulfuric acid. Sulfonations, cleavage and hydrolysis reactions often employ hot sulfuric acid. The most corrosive concentration for hot aqueous solutions of sulfuric acid appears to be about 55 sulfuric acid.
  • Prior art alloys are poor in corrosion resistance in the presence of either or both hot phosphoric acid and hot sulfuric acid. Usually resistance to sulfuric acid corrosion is readily attained, but the characteristic of resistance to corrosion by hot phospohric acid is difiicult to add. Even more diflicult is to retain these corrosion resistant characteristics in an alloy that is ductile and can be worked sufficiently so that it can be used without sole reliance upon casting as the method of shaping.
  • the metal alloy of this invention has the above desirable characteristics. It is a tantalum base alloy comprised by Weight of about 10 to 30% titanium, 3 to 10% vanadium and 0.25 to 3% nickel. Preferably, for good workability and ductility, the alloy contains 20 to 25% titanium and 5 to 7.5% vanadium. Without vanadium, a tantalum-titanium-nickel alloy was extremely difficult to work, either in cold rolling or hot rolling with protective cladding. *For use with the most corrosive hot phosphoric acid concentrations, i.e., about 85%, the alloy should contain at least 0.5%, and preferably about 1%, of nickel. Optionally, columbium and tungsten can be added.
  • Tungsten in amounts to serves to increase further the resistance to hydrogen embrittlement as well as to stabilize and to add strength to the alloy.
  • the alloy shoud contain no less than 30%, and preferably at least 50% of tantalum.
  • the carbon content of the alloy should be no more than 0.03%; the oxygen content, no more than about 0.05%; the nitrogen con-tent, no more than 0.008%; the hydrogen content, no more than about 0.001%.
  • the carbon content of the alloy should be no more than 0.03%; the oxygen content, no more than about 0.05%; the nitrogen con-tent, no more than 0.008%; the hydrogen content, no more than about 0.001%.
  • the resulting metal sandwiches of alloys were rolled at 2000 The rolling was done in a Stana-t two-high mill and the metal was reduced 7.5% to 15% per pass to a total of about
  • the alloys were tested for corrosion by exposing them to solutions of 55% sulfuric acid and phosphoric acid sealed in heavy-wall Pyrex ampules. Alloy specimens were prepared by grinding, sanding and finishing of surfaces and edges, and degreasing. Surface areas (generally about 6.5 cm. weights and densities were then determined. The density was measured by weight-in weight-out of water method. The volumes of sulfuric acid and phosphoric acid solutions were 40 and 30 ml., respectively.
  • alloys Nos. 1 and 2 without nickel the high penetration or corrosion rates in phosphoric acid show considerable hydrogen embrittlement.
  • alloy compositions 3, 4 and 5 were ductile and were readily hot rolled to give slight weight gains in the corrosion tests.
  • the weight gain shows the formation of an insoluble protective film on the metal surface.
  • the weight gain becomes constant. For example, alloy No. 5, upon exposure to 85% phosphoric acid at 400 F. gained no further weight after continuing the run for 164 hours. Testing alloy No. 5 under the same conditions for a total of 336 hours showed that the constant weight was attained in 48 hours. Similarly, alloy No. 4 when tests in 55% sulfuric acid at 450 F.
  • a ductile metal composition resistant to the action of hot oxidizing and non-oxidizing acids consisting essentially of, in percent by weight, 1030% of titanium, 3-10% of vanadium, .25 to 3% of nickel, up to 25 columbium, up to 10 tungsten, and the balance essentially tantalum, with the tantalum being present in an amount of at least 2.
  • a ductile metal composition resistant to the action of hot oxidizing and non-oxidizing acids consisting essentially of, in percent by weight, 20-25% of titanium, 5-7.5% of vanadium, 0.5 to 3% of nickel, up to 25% columbi-um, up to "10% tungsten, and the balance essentially tantalum, with the tantalum being present in an amount of at least References Cited in the file of this patent UNITED STATES PATENTS 1,588,518 Brace June 15, 1926 2,964,399 Lyons Dec. 13, 1960 FOREIGN PATENTS 803,855 Great Britain Apr. 3, 1957 201,297 Austria Dec. 27, 1958

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Pressure Welding/Diffusion-Bonding (AREA)
  • Arc Welding In General (AREA)

Description

United States Patent 3,128,178 TANTALUM-TTTANIUM BASE ALLQY Edward F. Dutieir, in, Mountain View, Qalit, assignor to California Research florporation, an Francisco, Calif.,
a corporation of Delaware No Drawing. Filed Feb. 28, 1961, Ser. No. 92,151 2 Claims. (=Cl. 75--174) This invention relates to tantalum-titanium base metal alloys, particularly to such alloys which contain alloying metals of vanadium and nickel as essential components, which make the resulting alloys ductile and resistant to corrosion by hot oxidizing and hot non-oxidizing acids.
Alloys with the above properties are most useful for lining chemical reaction vessels, auxiliary equipment and connecting lines, which are exposed to hot phosphoric acid and hot sulfuric acid. Liquid phosphoric acid is recognized as an efficient catalyst for certain organic chemical reactions, including alkylation and isomerization and the polymerization of normally gaseous olefins. Corrosive attack appears to be the greatest with aqueous solutions of about 85% phosphoric acid. While considerable progress has been made in controlling corrosion in the presence of liquid phosphoric acid (see, for example, Kemp and Zeh Patent 2,65 3,177 and Piehl Patent 2,854,- 497), there is need for further improvement and particularly for alloys which are also resistant to corrosion in the presence of hot oxidizing acids such as sulfuric acid. Sulfonations, cleavage and hydrolysis reactions often employ hot sulfuric acid. The most corrosive concentration for hot aqueous solutions of sulfuric acid appears to be about 55 sulfuric acid.
Prior art alloys are poor in corrosion resistance in the presence of either or both hot phosphoric acid and hot sulfuric acid. Usually resistance to sulfuric acid corrosion is readily attained, but the characteristic of resistance to corrosion by hot phospohric acid is difiicult to add. Even more diflicult is to retain these corrosion resistant characteristics in an alloy that is ductile and can be worked sufficiently so that it can be used without sole reliance upon casting as the method of shaping.
The metal alloy of this invention has the above desirable characteristics. It is a tantalum base alloy comprised by Weight of about 10 to 30% titanium, 3 to 10% vanadium and 0.25 to 3% nickel. Preferably, for good workability and ductility, the alloy contains 20 to 25% titanium and 5 to 7.5% vanadium. Without vanadium, a tantalum-titanium-nickel alloy was extremely difficult to work, either in cold rolling or hot rolling with protective cladding. *For use with the most corrosive hot phosphoric acid concentrations, i.e., about 85%, the alloy should contain at least 0.5%, and preferably about 1%, of nickel. Optionally, columbium and tungsten can be added. Up to 15%, and sometimes up to 25%, of columbium can be used where lighter weight is an important factor. Tungsten in amounts to serves to increase further the resistance to hydrogen embrittlement as well as to stabilize and to add strength to the alloy. However, the alloy shoud contain no less than 30%, and preferably at least 50% of tantalum.
We have found that, as compared to high temperature air oxidation, corrosion in aqueous conditions such as with the above aqueous acids is much more sensitive to impurities in the metal components of the alloy. Hence, impurities in the alloy should be kept to a minimum for the best results. Most desirably, the carbon content of the alloy should be no more than 0.03%; the oxygen content, no more than about 0.05%; the nitrogen con-tent, no more than 0.008%; the hydrogen content, no more than about 0.001%. 'In addition, no more than about 0.3% of the combined elements aluminum, chromium,
3,128,178 Patented Apr. 7, 1964 controlled atmospheres of argon, helium and the like are employed. Arc furnaces with water-cooled copper hearths and non-consumable electrodes (e.g. 2% thoriatedtungsten tip) were used in the preparations described below. Measured amounts of the metal components were The alloy compositions, all in terms of weight percent, were melted, the button of alloy inverted, and remelted four times before final cooling and solidifying. Alternatively, other furnaces and known melting techniques such as with continuous feed of metal components, inductive heating, or other means could be used with adequate protection against contamination.
In the folloding illustrative examples, most of the all'oys'were clad in 310 stainless steel to avoid oxidation at the high temperatures used in fabrication. Cladding was done by lathe machining the alloy button into circular discs, enclosing them inside a 3 x 3 x A-inch steel sheet having a circular hole in the middle, and welding 2% x 2% x As-inch steel plates on each side. The resulting metal sandwiches of alloys were rolled at 2000 The rolling was done in a Stana-t two-high mill and the metal was reduced 7.5% to 15% per pass to a total of about The alloys were tested for corrosion by exposing them to solutions of 55% sulfuric acid and phosphoric acid sealed in heavy-wall Pyrex ampules. Alloy specimens were prepared by grinding, sanding and finishing of surfaces and edges, and degreasing. Surface areas (generally about 6.5 cm. weights and densities were then determined. The density was measured by weight-in weight-out of water method. The volumes of sulfuric acid and phosphoric acid solutions were 40 and 30 ml., respectively. C-ontaminations due to silica formation in the phosphoric acid tests were avoided by liners of Teflon tubing inside the glass ampules. The corrosion tests were for 72 hours. From the measurements of weight loss, density and surface area, the penetration or corrosion rates in mils per year (i.e., m.p.y.) were determined.
The following table shows the results of tests carried out as described above:
Composition, percent Corrosion rates,
by weight In.p.y.
Number 557 857 Ta Ti v Ni rnsoi at Hard, at
25 5 0 2.5 67. 25 7. 5 0 2.5 61. 25 5 1 Wt. Wt.
galn. gain. 25 7. 5 1 d0 D03 25 5 2 do Do.
1 Weight gain of about .001 gms/cmfl. 2 Weight gain of about .003 gms./cm.
The above tests illustrate the need for nickel in the composition. In alloys Nos. 1 and 2 without nickel, the high penetration or corrosion rates in phosphoric acid show considerable hydrogen embrittlement. On the other hand, alloy compositions 3, 4 and 5 were ductile and were readily hot rolled to give slight weight gains in the corrosion tests. The weight gain shows the formation of an insoluble protective film on the metal surface. The weight gain becomes constant. For example, alloy No. 5, upon exposure to 85% phosphoric acid at 400 F. gained no further weight after continuing the run for 164 hours. Testing alloy No. 5 under the same conditions for a total of 336 hours showed that the constant weight was attained in 48 hours. Similarly, alloy No. 4 when tests in 55% sulfuric acid at 450 F. for a total of 168 hours reached a constant weight in about 48 hours. Unalloyed tantalum or the tantalum alloys Nos. 1 and 2 above show under such conditions a steadily increasing weight loss. The alloys of the present invention are therefore superior since corrosion and hence hydrogen embrittlement are minimized.
For comparison, an alloy without titanium and composed of 74% tantalum, 25 vanadium and 1% nickel recrystallized and cracked on attempted rolling at 2000 F. after cladding. Further, solutionizing of this alloy for 68 hours at 1900 F. did not improve the workability.
Other ductile tantalum-titanium base alloys which illustrate the corrosion resistance (to hot sulfuric and phosphoric acids) alloy compositions of the present in vention are tabulated as follows:
[Cmpositlon, percent by weight] These various ductile, corrosion resistant alloys of the present invention are preferably used as lining materials for vessels and other equipment. They can be applied after rolling or other suitablejabricating manner by conventional methods of welding, brazing, vacuum joining, and the like.
I claim:
1, A ductile metal composition resistant to the action of hot oxidizing and non-oxidizing acids and consisting essentially of, in percent by weight, 1030% of titanium, 3-10% of vanadium, .25 to 3% of nickel, up to 25 columbium, up to 10 tungsten, and the balance essentially tantalum, with the tantalum being present in an amount of at least 2. A ductile metal composition resistant to the action of hot oxidizing and non-oxidizing acids and consisting essentially of, in percent by weight, 20-25% of titanium, 5-7.5% of vanadium, 0.5 to 3% of nickel, up to 25% columbi-um, up to "10% tungsten, and the balance essentially tantalum, with the tantalum being present in an amount of at least References Cited in the file of this patent UNITED STATES PATENTS 1,588,518 Brace June 15, 1926 2,964,399 Lyons Dec. 13, 1960 FOREIGN PATENTS 803,855 Great Britain Apr. 3, 1957 201,297 Austria Dec. 27, 1958

Claims (1)

1. A DUCTILE METAL COMPOSITION RESISTANT TO THE ACTION OF HOT OXIDIZING AND NON-OXIDIZING ACIDS AND CONSISTING ESSENTIALLY OF, IN PERCENT BY WEIGHT, 10-30% OF TITANIUM, 3-10% OF VANADIUM, .25 TO 3% OF NICKEL, UP TO 25% COLUMBIUM, UP TO 10% TUNGSTEN, AND THE BALANCE ESSENTIALLY TANTALUM, WITH THE TANTALUM BEING PRESENT IN AN AMOUNT OF AT LEAST 30%.
US92151A 1961-02-28 1961-02-28 Tantalum-titanium base alloy Expired - Lifetime US3128178A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US92151A US3128178A (en) 1961-02-28 1961-02-28 Tantalum-titanium base alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US92151A US3128178A (en) 1961-02-28 1961-02-28 Tantalum-titanium base alloy

Publications (1)

Publication Number Publication Date
US3128178A true US3128178A (en) 1964-04-07

Family

ID=22231879

Family Applications (1)

Application Number Title Priority Date Filing Date
US92151A Expired - Lifetime US3128178A (en) 1961-02-28 1961-02-28 Tantalum-titanium base alloy

Country Status (1)

Country Link
US (1) US3128178A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3249429A (en) * 1963-12-27 1966-05-03 Clo E Armantrout Tantalum brazing alloy
US3293741A (en) * 1964-04-20 1966-12-27 Ralph G Gilliland Brazing alloys for refractory metals
US3449118A (en) * 1966-11-15 1969-06-10 Us Navy Vanadium-columbium-tantalum alloys
US4496373A (en) * 1981-12-11 1985-01-29 Kernforschungsanlage Julich Gesellschaft Mit Beschrankter Haftung Diffusion membrane and process for separating hydrogen from gas mixture
US20060153729A1 (en) * 2005-01-13 2006-07-13 Stinson Jonathan S Medical devices and methods of making the same
US20070276488A1 (en) * 2003-02-10 2007-11-29 Jurgen Wachter Medical implant or device
US20080038146A1 (en) * 2003-02-10 2008-02-14 Jurgen Wachter Metal alloy for medical devices and implants
US20080312740A1 (en) * 2003-02-10 2008-12-18 Jurgen Wachter Metal alloy for medical devices and implants

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1588518A (en) * 1919-04-18 1926-06-15 Westinghouse Electric & Mfg Co Alloy of tantalum
GB803855A (en) * 1957-04-03 1958-11-05 Du Pont Improvements in or relating to niobium alloys
AT201297B (en) * 1957-10-11 1958-12-27 Plansee Metallwerk Refractory sintered alloy
US2964399A (en) * 1959-06-25 1960-12-13 Titanium Metals Corp Tantalum-titanium corrosion resistant alloy

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1588518A (en) * 1919-04-18 1926-06-15 Westinghouse Electric & Mfg Co Alloy of tantalum
GB803855A (en) * 1957-04-03 1958-11-05 Du Pont Improvements in or relating to niobium alloys
AT201297B (en) * 1957-10-11 1958-12-27 Plansee Metallwerk Refractory sintered alloy
US2964399A (en) * 1959-06-25 1960-12-13 Titanium Metals Corp Tantalum-titanium corrosion resistant alloy

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3249429A (en) * 1963-12-27 1966-05-03 Clo E Armantrout Tantalum brazing alloy
US3293741A (en) * 1964-04-20 1966-12-27 Ralph G Gilliland Brazing alloys for refractory metals
US3449118A (en) * 1966-11-15 1969-06-10 Us Navy Vanadium-columbium-tantalum alloys
US4496373A (en) * 1981-12-11 1985-01-29 Kernforschungsanlage Julich Gesellschaft Mit Beschrankter Haftung Diffusion membrane and process for separating hydrogen from gas mixture
US20080038146A1 (en) * 2003-02-10 2008-02-14 Jurgen Wachter Metal alloy for medical devices and implants
US20070276488A1 (en) * 2003-02-10 2007-11-29 Jurgen Wachter Medical implant or device
US20080312740A1 (en) * 2003-02-10 2008-12-18 Jurgen Wachter Metal alloy for medical devices and implants
US20100222866A1 (en) * 2003-02-10 2010-09-02 Jurgen Wachter Metal alloy for medical devices and implants
US8349249B2 (en) 2003-02-10 2013-01-08 Heraeus Precious Metals Gmbh & Co. Kg Metal alloy for medical devices and implants
US8403980B2 (en) 2003-02-10 2013-03-26 Heraeus Materials Technology Gmbh & Co. Kg Metal alloy for medical devices and implants
US20060153729A1 (en) * 2005-01-13 2006-07-13 Stinson Jonathan S Medical devices and methods of making the same
US7727273B2 (en) 2005-01-13 2010-06-01 Boston Scientific Scimed, Inc. Medical devices and methods of making the same
US20100228336A1 (en) * 2005-01-13 2010-09-09 Stinson Jonathan S Medical devices and methods of making the same
US7938854B2 (en) 2005-01-13 2011-05-10 Boston Scientific Scimed, Inc. Medical devices and methods of making the same

Similar Documents

Publication Publication Date Title
US3785787A (en) Stainless steel with high resistance against corrosion and welding cracks
US4533414A (en) Corrosion-resistance nickel alloy
US3128178A (en) Tantalum-titanium base alloy
CA1214667A (en) Duplex alloy
Ogawa et al. The weldability of nitrogen-containing austenitic stainless steel: Part II—Porosity, cracking and creep properties
US4545826A (en) Method for producing a weldable austenitic stainless steel in heavy sections
Baeslack III et al. Selection and weldability of conventional titanium alloys
US3186837A (en) Columbium-tantalum base alloy
JPS582265B2 (en) Ferrite Goukin
US4832765A (en) Duplex alloy
US3984239A (en) Filler metal
US5296054A (en) Austenitic steel
US3597193A (en) Vanadium base alloy
US3249429A (en) Tantalum brazing alloy
US4050928A (en) Corrosion-resistant matrix-strengthened alloy
JPH0598394A (en) High v-containing high nitrogen ferritic heat resistant steel and its manufacture
US3672876A (en) Ductile corrosion-resistant ferrous alloys containing chromium
US4279650A (en) Titanium bearing addition alloys
US3212886A (en) High temperature alloy
US3676226A (en) High strength copper-nickel alloy
JPH0598393A (en) High nb-containing high nitrogen ferritic heat resistant steel and its manufacture
US2805153A (en) High tensile vanadium alloys
JPS6221855B2 (en)
Weare et al. Welding and brazing of molybdenum
US3627513A (en) Hydrochloric acid resistant ferrous alloy containing nickel copper and tungsten