Barium and lithium ratio for flux cored electrode

Information

  • Patent Grant
  • 7812284
  • Patent Number
    7,812,284
  • Date Filed
    Tuesday, July 12, 2005
    19 years ago
  • Date Issued
    Tuesday, October 12, 2010
    14 years ago
Abstract
Various slag systems exhibiting improved flow characteristics and weld puddle properties are provided. Also provided are flux cored electrodes for producing the noted slag systems and related methods of arc welding.
Description

The present invention relates to particular ratios of barium and lithium for flux cored electrodes such as used in a variety of arc welding processes.


BACKGROUND OF INVENTION

In the field of arc welding, the main types of welding processes are gas-metal arc welding with solid (GMAW) or metal cored wires (GMAW-C), gas shielded flux-cored arc welding (FCAW-G), self-shielded flux-cored arc welding (FCAW-S), shielded metal arc welding (SMAW) and submerged arc welding (SAW).


Metal cored electrodes are used increasingly as an alternative to solid wires because of increased productivity during welding fabrication of structural components. Metal cored electrodes are composite electrodes consisting of a core (fill) material surrounded by a metallic outer sheath. The core consists mainly of iron powder and alloying and fluxing ingredients to help with arc stability, weld wetting and appearance etc., such that the desired appearance and mechanical properties are obtained in the weld. Metal cored electrodes are manufactured by mixing the ingredients of the core material and depositing them inside a formed strip, and then closing and drawing the strip to the final diameter. Metal cored electrodes provide increased deposition rates and produce a wider, more consistent weld penetration profile compared to solid electrodes. Moreover, they provide improved arc action, generate less fume and spatter, and provide weld deposits with better wetting compared to solid electrodes.


FCAW-S electrodes do not use any shielding during welding and protection of the weld metal from the ambient is achieved through the use of deoxidizers and dentriders like Al, Mg, Ti and Zr. However, a certain ratio of barium to lithium is often utilized in order to control the melting range and the fluidity of the slag and weld puddle. This ratio can be modified to render the electrode appropriate for welding out of position, i.e. either vertically up or vertically down. From ternary diagrams of barium, lithium and strontium fluorides, it is known that melting point is generally reduced with increasing levels of lithium fluoride.


Although electrodes with barium and lithium compounds are known, a need still remains for electrode and resulting slag compositions that exhibit improved properties, particularly with respect to the proportions of barium and lithium and the flow characteristics of the slag and weld puddle properties resulting therefrom.


THE INVENTION

In a first aspect, the present invention provides a flux cored electrode in which the components of the core are chosen to produce a particular slag system. The core components include from about 35% to about 55% barium fluoride, and from about 2% to about 12% lithium fluoride.


In another aspect, the present invention provides a flux cored electrode comprising barium and lithium in a mass ratio of total barium to total lithium of from about 8:1 to about 12:1.


In yet another aspect, the present invention provides a slag system resulting from a flux cored electrode, the slag system resulting from the presence of from about 35% to about 55% barium fluoride and from about 2% to about 12% lithium fluoride in the core of the electrode.


In yet another aspect, the present invention provides a method of arc welding using a flux cored electrode. The method comprises providing a flux cored electrode that produces a slag system resulting from the presence of (i) from about 35% to about 55% barium fluoride and (ii) from about 2% to about 12% lithium fluoride in the core of the electrode. The method also comprises passing an electric current through the electrode to thereby produce the slag system.


In yet another aspect, the present invention provides a method of arc welding using a flux cored electrode. The method comprises providing a flux cored electrode that includes barium and lithium in a mass ratio of total barium to total lithium of from about 8:1 to about 12:1. The method also comprises passing an electric current through the electrode to thereby produce the slag system.


These and other objects and advantages will become apparent from the following description.







PREFERRED EMBODIMENTS

The present invention is based upon a discovery that excellent properties in a resulting slag can be obtained if barium and lithium are utilized in certain proportions, in the slag. Accordingly, various preferred embodiment slag systems, electrode compositions for forming such slag systems, and related methods of use are provided.


A preferred electrode composition in accordance with the present invention comprises:

    • barium fluoride, as the barium source, from about 35 to about 55% of the core material (by weight),
    • lithium fluoride, as the lithium source, from about 2 to about 12% of the core material (by weight),
    • barium carbonate, as a secondary barium source, from about 0 to about 8% of the core material (by weight),
    • lithium carbonate, as the secondary lithium source, from about 0 to about 8% of the core material (by weight) as lithium carbonate,
    • lithium oxide, from about 2 to about 15% of the core material,
    • iron oxide, from about 5 to about 20% of the core material,
    • calcium oxide, from about 0 to about 5% of the core material,
    • silicon oxide, from about 0 to about 5% of the core material,
    • manganese oxide, from about 0 to about 5% of the core material,
    • aluminum, magnesium, titanium, zirconium, or combinations thereof, up to about 25% of the core material, for deoxidation and denitriding, and
    • the remaining core material including metallics such as, but not limited to iron, nickel, manganese and/or silicon.


Preferably, a barium to lithium ratio from about 8:1 to about 12:1, respectively, is utilized for optimum weldability and good operating range. This ratio is the mass ratio of total barium to total lithium in the electrode. A ratio less than about 8:1 will cause poor arc action while a ratio greater than about 12:1 will cause poor voltage range and produce welds with porosity.


Set forth below in Table 1 is a representative core formulation of a flux cored electrode used for forming the preferred slag systems. All percentages in Table 1 are based upon the weight of the electrode core formulation, which in turn constitutes about 20% of the electrode by weight.









TABLE 1





Representative Core Formulation


















Al
15.371



C
0.023



Co
0.021



Cu
0.018



Fe
10.066



Mg
3.921



Mn
5.166



Na
0.008



Nb
0.003



Ni
4.102



P
0.006



Pb
0.004



S
0.062



Si
0.049



Sn
0.004



Ti
0.011



Zn
0.018



Zr
0.786



Al2O3
0.364



CaO
1.8



Fe2O3
17.802



K2O
0.205



Li2O
0.758



SiO2
4.3



TiO2
0.019



BaF2
27.819



K2SiF6
0.975



LiF
5.258



NaF
0.002



SrF2
4.972










The preferred embodiment slag systems and electrodes for forming such systems can employ a wide range of compounds used in the electrode for providing a source of barium in the resulting slag. For example, it is contemplated that barium monoferrate (BaFe2O4) and complexes of BaO, Fe2O3, CaO, SiO2, and/or TiO2 can be used in the electrode. Although generally less preferred due to its strong hygroscopic properties, BaO by itself, could in certain embodiments, be used in the electrode.


The preferred embodiment slag systems and electrodes for forming such systems can utilize a wide array of compounds used in the electrode for providing a source of lithium in the resulting slag. For example, it is contemplated that various complexes of Li2O, Fe2O3, MnO2, CaO, SiO2, and/or TiO2 can be used in the electrode. Although generally less preferred due to its strong hygroscopic properties, Li2O by itself, could in certain embodiments be used in the electrode.


The levels of barium and lithium fluoride were changed to evaluate the effect of these individual slag-making agents on arc stability and resistance to porosity. Automated weld tests at sequentially increasing voltages in the vertical down position were used to evaluate the operating range of an electrode product. Increasing barium fluoride additions made the weldability of the electrode better, but did not improve the operable range of the electrode. Increasing lithium fluoride increased the voltage range of the electrode in an automated robotic test. Decreasing lithium fluoride decreased the operating range of the electrode.


The present development is particularly directed to providing electrodes, and particularly flux cored electrodes for arc welding, that utilize relatively large amounts of barium and lithium fluorides. Although the development includes electrodes with barium and/or lithium carbonates, the development is primarily directed to electrode compositions in which barium and lithium fluorides are the major components, and such fluorides being in optional combination with minor amounts of barium and/or lithium carbonates.


Additional details of arc welding materials and specifically, cored electrodes for welding are provided in U.S. Pat. Nos. 5,369,244; 5,365,036; 5,233,160; 5,225,661; 5,132,514; 5,120,931; 5,091,628; 5,055,655; 5,015,823; 5,003,155; 4,833,296; 4,723,061; 4,717,536; 4,551,610; and 4,186,293; all of which are hereby incorporated by reference.


The foregoing description is, at present, considered to be the preferred embodiments of the present invention. However, it is contemplated that various changes and modifications apparent to those skilled in the art, may be made without departing from the present invention. Therefore, the foregoing description is intended to cover all such changes and modifications encompassed within the spirit and scope of the present invention, including all equivalent aspects.

Claims
  • 1. A flux cored electrode having a sheath and core materials in the metal sheath, said core materials including barium fluoride, lithium fluoride, lithium oxide, aluminum, and iron oxide, said core materials including about 35-55 weight percent barium fluoride, about 2-12 weight percent lithium fluoride, about 2-12 weight percent lithium oxide, about 15 weight percent aluminum, and about 5-20 weight percent iron oxide, a weight ratio of a total weight percent of barium to a total weight percent of lithium in said core materials is about 8-12:1.
  • 2. The flux cored electrode as defined in claim 1, wherein said core materials include at least one oxide selected from the group consisting of calcium oxide, silicon oxide, manganese oxide, and mixtures thereof, said calcium oxide constituting up to about 5 weight percent of said core materials, said silicon oxide constituting up to about 5 weight percent of said core materials, said manganese oxide constituting up to about 5 weight percent of said core materials.
  • 3. The flux cored electrode as defined in claim 1, wherein said core materials include at least one metal agent selected from the group consisting of aluminum, magnesium, titanium, zirconium, and mixtures thereof, said metal agent constituting up to about 25 weight percent of said core materials.
  • 4. The flux cored electrode as defined in claim 1, wherein said core materials include at least one metal agent selected from the group consisting of iron, nickel, manganese, silicon, and mixtures thereof.
  • 5. The flux cored electrode as defined in claim 1, wherein said core materials include barium fluoride, calcium oxide, iron oxide, lithium fluoride, silicon oxide, aluminum, iron, magnesium, and manganese.
  • 6. The flux cored electrode as defined in claim 5, wherein said core materials include barium fluoride, calcium oxide, iron oxide, lithium fluoride, lithium oxide, silicon oxide, strontium fluoride, aluminum, iron, magnesium, manganese, nickel, and zirconium.
  • 7. The flux cored electrode as defined in claim 6, wherein said core materials include aluminum oxide, barium fluoride, calcium oxide, iron oxide, lithium fluoride, lithium oxide, potassium silicofluoride, potassium oxide, silicon oxide, strontium fluoride, aluminum, iron, magnesium, manganese, nickel, and zirconium.
  • 8. The flux cored electrode as defined in claim 1, wherein said core materials include at least one secondary lithium source selected from the group consisting of lithium carbonate, lithium oxide, complexes including lithium oxide, and mixtures thereof.
  • 9. The flux cored electrode as defined in claim 1, wherein said core materials include barium carbonate, said barium carbonate constituting up to about 8 weight percent of said core materials.
  • 10. The flux cored electrode as defined in claim 1, wherein said core materials include lithium carbonate, said lithium carbonate constitutes up to about 8 weight percent of said core materials.
  • 11. The flux cored electrode as defined in claim 1, wherein said core materials include at least one secondary barium source selected from the group consisting of barium carbonate, barium monoferrate, barium oxide, complexes including barium oxide, and mixtures thereof.
US Referenced Citations (94)
Number Name Date Kind
2802762 Stetson et al Aug 1957 A
3177340 Danhier Apr 1965 A
3415976 Smith Dec 1968 A
3458685 Tezuka Jul 1969 A
3461270 Patton Aug 1969 A
3466417 Chapman Sep 1969 A
3539765 Duttera Nov 1970 A
3566073 Black Feb 1971 A
3585343 Crichton Jun 1971 A
3585352 Zvanut Jun 1971 A
3596053 Kameda Jul 1971 A
3627574 DeLong Dec 1971 A
3670135 Zvanut Jun 1972 A
3702390 Blake et al. Nov 1972 A
3742185 Parks Jun 1973 A
3767891 Haverstraw et al. Oct 1973 A
3769491 De Long et al. Oct 1973 A
3778588 Bishel Dec 1973 A
3778589 Nakabayashi Dec 1973 A
3786658 Kammer Jan 1974 A
3866015 Matsumoto Feb 1975 A
3883713 Gurevich May 1975 A
3911244 Nakamura Oct 1975 A
4010309 Peterson Mar 1977 A
4020320 Pijls Apr 1977 A
4072845 Buckingham Feb 1978 A
4122238 Frantzerb Oct 1978 A
4149063 Bishel Apr 1979 A
4154999 Pinfold et al. May 1979 A
4186293 Gonzalez et al. Jan 1980 A
4207454 Safonnikov et al. Jun 1980 A
4314136 Kotecki Feb 1982 A
4366364 Giese Dec 1982 A
4376881 Safonnikov et al. Mar 1983 A
4449031 Kotecki May 1984 A
4454406 Safonnikov et al. Jun 1984 A
4465036 Sakai et al. Aug 1984 A
4465921 Sakai Aug 1984 A
4510374 Kobayashi Apr 1985 A
4512822 Barringer et al. Apr 1985 A
4551610 Amata Nov 1985 A
4557768 Barringer et al. Dec 1985 A
4571480 Sakai et al. Feb 1986 A
4689461 Gamberg Aug 1987 A
4717536 Chai et al. Jan 1988 A
4723061 Munz Feb 1988 A
4800131 Marshall Jan 1989 A
4803340 Sato Feb 1989 A
4833296 Crockett et al. May 1989 A
4889969 Kawai Dec 1989 A
4948936 Landry Aug 1990 A
4999479 Paton Mar 1991 A
5003155 Chai Mar 1991 A
5015823 Crockett May 1991 A
5055655 Chai Oct 1991 A
5091628 Chai Feb 1992 A
5120931 Kotecki Jun 1992 A
5124529 Nishikawa Jun 1992 A
5124530 O'Donnell Jun 1992 A
5132514 Chai Jul 1992 A
5225661 Chai Jul 1993 A
5233160 Gordish Aug 1993 A
5304346 O'Donnell Apr 1994 A
5308698 Bishel May 1994 A
5365036 Crockett Nov 1994 A
5369244 Kulikowski Nov 1994 A
5861605 Ogawa Jan 1999 A
5914061 Ogawa Jun 1999 A
6124569 Bonnet Sep 2000 A
6300596 Bonnet Oct 2001 B1
6337144 Shimizu Jan 2002 B1
6340396 Ogawa Jan 2002 B1
6441334 Aida Aug 2002 B1
6521867 Bonnet Feb 2003 B2
6573476 Kim Jun 2003 B2
6649872 Kato Nov 2003 B2
6713723 Lee Mar 2004 B2
6723954 Nikodym Apr 2004 B2
6841246 Shimizu Jan 2005 B2
7271365 Stava et al. Sep 2007 B2
20010023863 Bonnet Sep 2001 A1
20020037420 Shimizu Mar 2002 A1
20020043307 Ishida Apr 2002 A1
20020060212 Kim May 2002 A1
20030094444 Kato May 2003 A1
20030116234 Santella Jun 2003 A1
20030116550 Lee Jun 2003 A1
20040020912 Hara Feb 2004 A1
20040187961 Crockett Sep 2004 A1
20040188407 Nikodym Sep 2004 A1
20040256370 Keegan Dec 2004 A1
20050121110 Dallam et al. Jun 2005 A1
20060070983 Narayanan et al. Apr 2006 A1
20070170163 Narayanan Jul 2007 A1
Foreign Referenced Citations (19)
Number Date Country
0120920 Oct 1984 EP
0125925 Nov 1984 EP
0231570 Aug 1987 EP
0231570 Aug 1987 EP
774317 Feb 2002 EP
1297865 Nov 1972 GB
1297865 Nov 1972 GB
1397685 Jun 1975 GB
2020591 Nov 1979 GB
2020591 Nov 1979 GB
2155045 Sep 1985 GB
6-023547 Feb 1985 JP
05228691 Sep 1993 JP
05237693 Sep 1993 JP
2000126893 May 2000 JP
2000301382 Oct 2000 JP
20000288730 Oct 2000 JP
1780979 Dec 1992 RU
1826 338 Aug 1996 RU
Related Publications (1)
Number Date Country
20070012673 A1 Jan 2007 US