Methods of making a coated cemented carbide body include: forming a powder mixture having wc, 5-12 wt % Co, 3-11% cubic carbides of Ta and ti with a ratio of Ta/ti is 1.0-4.0; adding N in an amount of 0.6-2.0% of the weight of Ta and ti; milling and spray-drying the mixture to form a powder; compacting and sintering the powder at a temperature of 1300-1500° C., in a controlled atmosphere of about 50 mbar followed by cooling, whereby a body having a binder phase enriched and essentially gamma-phase free surface zone of 5-50 μm in thickness is obtained; applying a pre-coating treatment to the body; and appling a hard, wear-resistant coating to the body.

Patent
   RE40962
Priority
Apr 08 1999
Filed
Jul 10 2006
Issued
Nov 10 2009
Expiry
Apr 07 2020
Assg.orig
Entity
Large
0
32
all paid
1. A method of making a coated cemented carbide body having a gamma phase-free and binder rich surface zone comprising the steps of:
(i) forming a powder mixture comprising wc, 5-12 wt. % Co, 3-11 wt. % cubic carbides of Ta and ti, where the ratio of Ta/ti is 1.0-4.0;
(ii) adding N in an amount of 0.6-2.0% of the weight of Ta and ti;
(iii) milling and spray drying the mixture to form a powder material with the desired properties;
(iv) compacting and sintering the powder material at a temperature of 1300-1500° C., in a controlled atmosphere of about 50 mbar followed by cooling, whereby a body having a binder phase enriched and essentially gamma phase free surface zone of 5-50 μm in thickness is obtained;
(v) applying a pre-coating treatment to the body; and
(vi) applying a hard, wear resistant coating.
2. The method of claim 1, further comprising adding a pressing agent and W to the powder mixture in an amount to give the body a CW ratio of 0.75-0.95, the CW ratio is expressed as CW ratio=Ms/(wt. % Co*0.0161), where Ms is the measured saturization magnetization of the body and wt. % Co is the weight percentage of Co in the cemented carbide.
3. The method according to claim 1, wherein the powder mixture comprises 7-10 wt. % of cubic carbides of the metals Ta and ti.
4. The method according to claim 1, wherein the coating is applied using a CVD-technique.
5. The method according to claim 1, wherein the coating is applied using a MT-CVD-technique.
0. 6. The method of claim 1, wherein the surface zone is approximately 10-30 μm thick.
0. 7. The method of claim 1, wherein the surface zone has a binder phase content 1.2-2.0 times the binder phase content in the rest of the body.
0. 8. The method of claim 1, wherein the Ta/ti-ratio is 2.0-3.0.
0. 9. The method of claim 2, wherein the CW ratio is 0.8-0.85.
0. 10. The method of claim 1, wherein the Co content is 9-11 wt. %.
0. 11. The method of claim 1, wherein the combined content of TaC and TiC is 3-11 wt. %.
0. 12. The method of claim 1, wherein the body comprises wc having a grain size of 1.0-4.0 μm.
0. 13. The method of claim 12, wherein the grain size is 1.5-3.0 μm.
0. 14. The method of claim 1, wherein the coating comprises a 3-12 μm columnar TiCN-layer, followed by a 1-8 μm thick Al2O3-layer.
0. 15. The method of claim 14, wherein the coating comprises an outermost layer of TiN.
0. 16. The method of claim 15, comprising removing the TiN layer at an edge line of the body.
0. 17. The method of claim 14, wherein the Al2O3-layer is κ-Al2O3.
0. 18. The method of claim 17, wherein the coating comprises an outermost layer of TiN.
0. 19. The method of claim 18, comprising removing the TiN layer at an edge line of the body.

Ms is the measured saturation magnetization of the cemented carbide body in kA/m hAm2/kg and wt-% Co is the weight percentage of Co in the cemented carbide. The CW-ratio takes a value less than or equal to 1. The lower the CW-ratio, the higher the W-content in the binder phase. It has now-been found according to the invention that an improved cutting performance is achieved if the CW-ratio is in the range 0.75-0.95, preferably 0.80-0.85.

The present invention is applicable to cemented carbides with a composition of 5-12, preferably 9-11, weight percent of Co binder phase, and 3-11, preferably 7-10, weight percent TaC+TiC, and the balance being WC. The Nb content should not exceed 0.1 weight percent. The weight ratio Ta/Ti should be 1.0-4.0, preferably 2.0-3.0. The WC preferably has an average grain size of 1.0 to 4.0 μm, more preferably 1.5 to 3.0 μm. The cemented carbide body may contain less than 1 volume % of η-phase (M6C).

Inserts according to the invention are further provided with a coating preferably comprising 3-12 μm columnar TiCN-layer followed by a 1-8 μm thick Al2O3-layer deposited, for example, according to any of the U.S. Pat. Nos. 5,766,782, 5,654,035, 5,974,564, 5,702,808, preferably a κ-Al2O3-layer and preferably with an outermost thin layer of TiN which preferably is removed in the edge line by brushing or by blasting.

According to the invention, by applying coatings with different thickness on the cemented carbide body the property of the coated insert can be optimised to suit specific cutting conditions.

In one embodiment, a cemented carbide insert produced according to the invention is provided with a coating of: 6 μm TiCN, 5 μm Al2O3 and 1 μm TiN. This coated insert is particularly suited for cutting operation in steel.

In another embodiment, a cemented carbide insert produced according to the invention is provided with a coating of: 4 μm TiN, 2 μm Al2O3 and 1 μm TiN. This coating is particularly suited for cutting operations in stainless steels.

The invention also relates to a method of making cutting inserts comprising a cemented carbide substrate of a binder phase of Co, WC, a gamma phase of Ta and Ti, a binder phase enriched surface zone essentially free of gamma phase, and a coating. A powder mixture containing 5-12, preferably 9-11, weight percent of binder phase consisting of Co, and 3-11, preferably 7-10, weight percent TaC+TiC, and the balance WC with an average grain size of 1.0-4.0 μm, more preferably 1.5-3.0 μm, is prepared. The Nb content should not exceed 0.1 weight percent. The weight ratio Ta/Ti should be 1.0-4.0, preferably 2.0-3.0. Well-controlled amounts of nitrogen have to be added either the powder as carbonitrides and/or added during the sintering process via the sintering gas atmosphere. The amount of nitrogen added will determine the rate of dissolution of the cubic phases during the sintering process and hence determine the overall distribution of the elements in the cemented carbide after solidification. The optimum amount of nitrogen to be added depends on the composition of the cemented carbide and, in particular, on the amount of cubic phases and varies between 0.6 and 2.0% of the weight of the elements Ti and Ta. The exact conditions depend to a certain extent on the design of the sintering equipment being used. It is within the purview of the skilled artisan to determine whether the requisite surface zone of the cemented carbide have been obtained and to modify the nitrogen addition and the sintering process in accordance with the present specification in order to obtain the desired result.

The raw materials are mixed with pressing agent and, optionally W, such that the desired CW-ratio is obtained. The mixture is milled and spray dried to obtain a powder material with the desired properties. Next, the powder material is compacted and sintered. Sintering is performed at a temperature of 1300-1500° C., in a controlled atmosphere of about 50 mbar followed by cooling. After conventional post sintering treatments, including edge rounding, a hard, wear resistant coating according to above is deposited by CVD- or MT-CVD-technique.

Metallographic investigation showed that the inserts had a gamma phase free zone of 15 μm. FIG. 1 shows a plot of the Co enrichment near the surface measured by an image analysis technique. The Co is enriched to a peak level of 1.3 times the bulk content. Magnetic saturation values were recorded and used for calculating CW-values. An average CW-value of 0.81 was obtained.

After a pre-coating treatment like edge honing, cleaning etc. The inserts were coated in a CVD-process comprising a first thin layer (less than 1 μm) of TiN followed by 6 μm thick layer of TiCN with columnar grains by using MTCVD-techniques (process temperature 850° C. and CH3CN as the carbon/nitrogen source). In a subsequent process step during the same coating cycle, a 5 μm thick κ-Al2O3 layer was deposited according to U.S. Pat. No. 5,974,564. On top of the κ-Al2O3 layer a 1.0 μm TiN layer was deposited. The coated inserts were brushed in order to smoothly remove the TiN coating from the edge line.

Metallographic investigation showed that the produced inserts had a gamma phase free zone of 12 μm. Magnetic saturation values were recorded and used for calculating CW-values. An average CW-value of 0.79 was obtained. The inserts were subject to the same pre-coating treatment as A, coated in the same coating process and also brushed in the same way as A.

Inserts from A, B and C were tested with respect to toughness in a longitudinal turning operation with interrupted cuts.

Cutting speed 130 m/min
Depth of cut 1.5 mm

Mean feed at breakage
Inserts A 0.31 mm/rev
Inserts B 0.22 mm/rev
Inserts C 0.22 mm/rev

Inserts from A, B and C were tested with respect to resistance to plastic deformation in longitudinal turning of alloyed steel (AISI 4340).

Cutting speed = 100 m/min
Feed = 0.7 mm/rev.
Depth of cut = 2 mm
Time in cut = 0.50 min

The plastic deformation was measured as the edge depression at the nose of the inserts.

Edge depression, μm
Insert A 49
Insert B 63
Insert C 62

Tests performed at an end user producing rear shaft for lorries. The inserts from A and C were tested in a three turning operations with high toughness demands due to interrupted cuts. The inserts were run until breakage of the edge. The inert style SNMG120412-PR was used.

Number of machined components
Operation 1 2 3
Variant A 172 219 119
Variant C 20 11 50

Examples 2, 3 and 4 show that the inserts A according to the invention surprisingly exhibit much better toughness in combination with somewhat better plastic deformation resistance in comparison to conventional inserts B and C.

The foregoing has described the principles, preferred embodiments and modes of operation of the present invention. However, the invention should not be construed as being limited to the particular embodiments discussed. Thus the above-described embodiments should be regarded as illustrative rather than restrictive, and it should be appreciated that variations may be made in those embodiments by workers skilled in the art without departing from the scope of the present invention as defined by the following claims.

Lenander, Anders, Lindholm, Mikael

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