T 0733/11 01-02-2013

Reasons for the Decision

1. The appeal is admissible.

2. Admissibility of the late-filed documents

2.1 Documents D6 to D12 were filed during the opposition proceedings but after the nine month opposition period. According to established case-law of the Boards of Appeal, 6th edition, 2010, VII.C.1.4.1, in proceedings before the opposition divisions, late-filed facts, evidence and arguments that went beyond the "indication of the facts, evidence and arguments" presented as part of the notice of opposition pursuant to Rule 76(c) EPC in support of the grounds of opposition on which the opposition was based should only exceptionally be admitted into the proceedings if, prima facie, there were reasons to suspect that such late-filed documents would prejudice the maintenance of the patent in suit. In any case, the opposition division is obliged to give reasons for its decision to disregard evidence not submitted in due time under Article 114(2) EPC, if the opponent remained of the view that it was relevant.

Thus, it has to be assessed on appeal whether the opposition division exercised its discretion not to admit documents D6 to D12 correctly.

2.2 In point 2 of the Reasons for the Decision, the opposition division gave detailed reasons as to why late-filed documents D6 to D12 were not considered more relevant than the timely submitted citations D1 to D5. For the following reasons, the Board concurs with the opposition division's assessment of the technical relevance of documents D6 to 12 with respect to the claimed subject matter.

D6 was published in 2004, i.e. after the priority date of 7 February 2003 of the patent at issue. This document does not, therefore, represent prior art within the meaning of Article 54 EPC.

D7 teaches that magnesium is added to nickel-based superalloys to improve high temperature ductility and low-cycle fatigue strength (D7, Introduction). Although D7 describes the behaviour of magnesium during electron-beam melting (EB), vacuum arc remelting (VAR) and electro-slag remelting (ESR), this document merely teaches that it is possible to add magnesium to the ingot when conducting electro-slag remelting. D7 neither discloses the composition of the claimed maraging steel nor the type and dimensions of the non-metallic inclusions defined in claim 1 of the patent at issue.

D8 does not deal with maraging steels. Rather, this document is concerned with the inclusion behaviour in special melting processes such as electron-beam melting, in particular with the effect of Mg in superalloys (D8, page 327, first column, first full paragraph). It also mentions TiN inclusions having a nucleus of MgO and a special state of TiN having surrounding carbides (D8, page 327, column 2, "Implications on superalloy processing").

D9 is not concerned with maraging steels either. Rather, this document describes a variety of analytical methods which generate chemical analysis and related information which can be used for identifying the type of inclusions in steels (D9, Conclusions).

D10 teaches the effect of deoxidising elements on a Fe-10% Ni alloy. This scientific publication describes the effect of primary deoxidation products of Al2O3, ZrO2, Ce2O3 and MgO on TiN precipitation in a Fe-10 wt%Ni alloy. Since the composition of the steel cited in D10 is different from that of the claimed maraging steel, it is not possible to assess the behaviour of TiN and MgO in the claimed alloy.

D11 discloses the composition of soft steel, which is different from that of the claimed maraging steel. The molten steel in D11 is deoxidized by adding magnesium under pressure and thereafter is subjected to a vacuum treatment. Specifically, the process of D11 aims at decreasing the amount of inclusions. However, nothing is taught in D11 about the size of the non-metallic inclusions, the content rate of inclusions having the spinel-form inclusions or consisting of alumina and how to control the amount of these inclusions.

D12, which is prior art under Article 54(3) EPC, has to be considered only with respect to novelty. However, this document fails to disclose maraging steels and is silent on the content rate of the spinel-form and alumina inclusions.

2.3 Given this situation and having regard to Article 12(4) of the Rules of Procedure of the Boards of Appeal of the EPO (RPBA), according to which it is in the Board's discretion to hold inadmissible facts, evidence or requests which were not admitted in the first instance, the Board decides not to admit documents D6 to D12 into the appeal proceedings either.

Hence, only documents D1 to D5 will be considered in the present decision.

3. Admission of the new ground of opposition under Article 100(b) EPC

The ground of opposition under Article 100(b) EPC was not raised by the appellant in its notice of opposition. In the appellant's view, the patent proprietor, in its response dated 17 July 2009 to the statement of the grounds of opposition, itself had admitted that the claimed process was insufficiently described. The new ground of opposition therefore arose from the patent proprietor's response.

Moreover, the new ground of opposition was evident from post-published document D6 originating from the patent proprietor. According to D6, specific parameters must be adhered to in order to obtain the claimed maraging steel. The appellant argued that in this situation and following the considerations given in G 10/91, the opposition division was obliged to introduce the new ground of opposition into the proceedings on its own motion.

3.1 It is evident from point 3 of the minutes of the oral proceedings held before the opposition division that the late-filed ground of opposition under Article 100(b) EPC was amply discussed with the parties. After deliberation, the chairman announced that this ground was not admitted. A detailed reasoning as to why the late-filed ground under Article 100(b) EPC was held inadmissible was given in point 3 of the impugned decision. After having considered the opponent's arguments and having regard to the considerations given in decision G 10/91, the opposition division held that the patent described at least one way of obtaining the maraging steel composition in a manner sufficiently clear and complete for it to be carried out by a person skilled in the art. The opposition division therefore decided not to admit the newly submitted ground into the opposition proceedings. The Board can see no reason to hold that the opposition division acted inappropriately in this regard.

3.2 The Board concurs with the assessment of the opposition division that the ground of insufficiency of disclosure, if relevant at all, could have been presented during the opposition period since the patent had not been amended and that it could not be derived for the first time from an interpretation of the patent proprietor's submissions in response to the grounds of opposition.

It is true that in point 2 of its response of 17 July 2009, the patent proprietor explained that the claimed steel was not obtained simply by specifying a specific amount of Mg and vacuum remelting the consumable electrode. In fact, other concomitant factors including the contents of inclusion-forming elements such as oxygen and nitrogen, the size and shape of the non-metallic inclusions contained in the consumable electrode and the rate of decomposition and crystallisation of the inclusions during remelting the consumable electrode could affect the final state of the inclusions in the maraging steel.

It is, however, to be noted that the examples given in the patent specification in paragraphs [0080] to [0087] and Table 1 describe in detail all the process steps for (a) producing the vacuum induction melted consumable electrode and (b) of the VAR step. As regards the VIM first step, the description mentions control of the size of Ti-carbonitride inclusions such as TiCN and TiN (not more than 10 mym), the cast rate (2.5), the coagulation speed and the nitrogen content (15 ppm) in the raw material (paragraphs [0081] to [0085]. Turning to the VAR second step, the degree of vacuum (1.3 Pa) and the projection current (6.5 KA) when remelting the consumable electrode during VAR are described. In addition, the chemical compositions of the consumable electrodes produced (a) by VIM and (b) of the steels obtained by VAR are listed in detail in Table 1. Contrary to the appellant's arguments, the patent specification therefore describes in detail the concrete process parameters of the method which enable the skilled person to put into practice the maraging steel defined in claims 1 and 2.

3.3 The appellant further alleged that the person skilled in the art could not produce the claimed steel without knowing the specific process conditions disclosed in document D6 which dealt with the same technical field.

However, document D6 was filed and published after the priority date of the present patent at issue and appears to be concerned with a further development of the process claimed in the patent at issue. Therefore, this document does not represent prior art under Article 54 EPC and, in consequence thereof, is not relevant to the present patent.

3.4 Given that the appellant's arguments are unfounded, the opposition division exercised its discretion correctly not to admit the new ground of opposition into the opposition proceedings. For the same reasons, the Board decides not to admit the new ground of opposition under Article 100(b) EPC into the appeal proceedings as well.

4. Novelty; Article 100(a) EPC

The appellant argued that the subject matter of claim 1 lacked novelty with respect to any of documents D1 to D3. For the following reasons, the Board cannot agree with the appellant's assessment.

4.1 Although the NiCoMo steel composition referred to in document D1, page 3, last paragraph, could optionally include 0 to 250 ppm Mg, none of the examples actually comprises magnesium as an alloying element which is required to be present in the claimed steel in amounts of greater than 0 but less than 10 ppm. Moreover, no information whatsoever is found anywhere in D1 about the size of the nitride and oxide inclusions and on the content rate of the spinel-form inclusions, as required in the claimed maraging steel.

As to the appellant's argument that example 9 of the patent at issue comprised 11 ppm Mg and fell outside the claimed range of greater than 0 and less than 10 ppm Mg, reference is made to paragraphs [0066] and [0067] of the patent specification. There, the skilled reader is taught that from the viewpoint of toughness magnesium should be restricted to less than 15 ppm, with less than 10 ppm Mg being preferred according to originally filed claims 5 and 6.

4.2 D2, like D3, discloses neither the type and size of the nitride and oxide inclusions nor the content rate of the spinel-form and alumina inclusions. Both documents remain silent on the low levels for oxygen and nitrogen that are necessary to control the amount of the non-metallic inclusions in the claimed steel.

The Board therefore concurs with the assessment of the opposition division that the subject matter of claim 1 is novel over any of documents D1 to D3.

4.3 As already pointed out in point 2.2. of this decision, the claimed subject matter is not anticipated by the technical disclosure of documents D11 and D12 either. Therefore, these documents are disregarded.

5. Inventive step; Article 100(a) EPC

The appellant argued that the claimed subject matter was obvious from D1, taken individually, or in combination with D3 or D5.

5.1 In fact, document D1 discloses the composition of a maraging steel comprising not more than 0.15% C, 14 to 22% Ni, 12 to 25% Co, 2 to 4% Mo, 0 to 0.4% Ti (preferably 0.05 to 0.2%), 0 to 0.4% Al, 0 to 0.025% Mg, up to 0.04% N (preferably less than 250 ppm N), oxygen as low as possible, the balance being Fe and incidental impurities (D1, pages 3 and 4). However, D1 remains silent on the cleanliness of the steel, in particular on the minimization or even elimination of non-metallic inclusions having a certain shape and structure.

As correctly pointed out by the appellant, the objective problem to be solved by the patent at issue, when starting from the technical disclosure of D1, resided in improving the steel's resistance to fatigue.

However, no pointer is found anywhere in D1 that by adding more than zero and less than 10 ppm Mg to the steel while simultaneously restricting the contents of oxygen and nitrogen to less than 10 ppm O and less than 15 ppm N the size and amounts of the non-metallic oxide and nitride inclusions were significantly reduced and that, in consequence thereof, the maraging steel exhibits a superior fatigue strength. This is all the more true since none of the examples in Table II of D1 even includes magnesium at all and defines the amounts of dissolved oxygen and nitrogen.

Document D3 is concerned with electroslag melting, refining and continuous casting of - amongst many other steels - maraging steels comprising 18 Ni. However, also D3 fails to give any hint or suggestion towards the problem to be solved by the patent at issue. In particular, on the basis of the technical teaching given in this document, the skilled person would not be prompted to add magnesium to the steel and to control the levels of oxygen and nitrogen within the claimed range so that the shape and amount of the non-metallic oxide and nitride inclusions in the steel is restricted to the range defined in claim 1 of the patent at issue.

D5 relates to producing maraging steels by vacuum induction melting a consumable electrode which in a second process step is re-melted by VAR (D5, page 4, lines 26 to 32). Contrary to D1 and also to the patent at issue, D5 aims a providing a cobalt-free maraging steel comprising up to 0.05% C, 0.5 to 4% Mo, 16.5 to 21% Ni, 1.25 to 2.5% Ti, up to 1% Al, balance Fe and incidental elements (D5, claim 1). Apart from Al, other deoxidising agents such as Zr, B, Ca and Mg could be added without, however, giving specific examples. Moreover, nothing is taught in D5 about the fatigue properties, the cleanliness of the steel and the specific effects of Mg, N and O on the formation of non-metallic inclusions. There is no reason to pick features from document D5 to associate with the teaching of D1 and even if this were done, the subject matter of claim 1 of the patent at issue would not be reached. Consequently, the subject matter of claim 1 is not obvious from the combination of technical teaching given in D5 and D1.

5.2 Hence, neither D1 taken individually or in combination with D3 nor the teaching given D5 combined with that of D1, respectively, would lead in an obvious way to the claimed maraging steel and its non-metallic inclusion chemistry.

5.3 It is further noted that the combination of documents D1 or D2, respectively, with document D11, also referred to by the appellant, would not lead to the claimed maraging steel either. Contrary to the technical teaching of document D1 disclosing the optional addition of 0 to 0.025% Mg, or to D2 which discloses the addition Ca and/or Mg in the range of 0.001 to 0.1% to improve the maraging steel's resistance to stress corrosion cracking, document D11 teaches to add calcium and/or magnesium under pressure as a deoxidation agent which is in the following vacuum treatment completely removed by vaporisation. Hence, the skilled person had no reason to combine the teaching of D1 or D2, respectively, with that of D11 and even if he did, the claimed steel composition would not be reached.

5.4 Consequently, the subject matter of claim 1 involves an inventive step.