T 0291/08 (Method of removing organic iodides/CELANESE) 13-01-2011

Reasons for the Decision

1. The appeal is admissible.

2. Reformatio in peius

The Appellant raised an objection based on the prohibition of reformatio in peius with respect to the main and the auxiliary request 1. However, in view of the outcome of these appeal proceedings which are in its favour (see below), a decision of the Board on this issue is unnecessary.

3. Remittal (Article 111(1) EPC)

3.1 The Respondent requested that the Board remit the case to the first instance on account of the new argument made during the oral proceedings by the Appellant, namely that document (8) was the closest prior art.

3.2 Pursuant to Article 111(1) EPC the Board may exercise any power within the competence of the first instance or remit the case to that department. Having arrived at the present stage of the appeal proceedings, the Board should therefore assess the appropriateness of a remittal.

3.3 In the present case, the examination as to the requirement of inventive step is made in respect of a document already taken into consideration in the decision under appeal, namely document (8). In the decision under appeal the Opposition Division decided that document (6) was the closest prior art, that means that the Opposition Division was of the opinion that document (6) was a more promising springboard for the invention than document (8). However, starting instead from document (8) as the closest prior art does not fundamentally change the factual framework of the case and hence does not justify a remittal to the first instance.

In the communication accompanying the summons to oral proceedings, the Board indicated to the Parties that they should be prepared to discuss whether document (8) represented the closest prior art. The Respondent, thus, had sufficient time to respond to an argument based on document (8) and in fact provided arguments as to why document (8) should not be taken as the closest prior art. Thus its right to be heard under Article 113(1) was not violated.

3.4 The justification put forward by the Respondent for its request to remit the case to the first instance was the right to have two instances. However, Article 111(1) EPC establishes no absolute right for Parties to have matters raised in appeal proceedings examined by two successive instances; on the contrary, it leaves the Board of Appeal to decide upon a remittal in the light of the circumstances (see inter alia T 133/87, point 2 of the reasons, not published in OJ EPO).

3.5 Under the present circumstances, the Respondent's request to remit the case to the first instance is thus refused.

Main request

4. Amendments (Article 123(2) and (3) EPC)

Claim 1 is based on the combination of original claims 10 and 15, which are identical to granted claims 13 and 18 respectively. Additionally the organic iodide to be removed is specified as being dodecyl iodide according to page 1, line 5 of the application as filed. The requirements of Article 123(2) and (3) EPC are thus satisfied.

5. Inventive step (Article 56 EPC)

According to the established jurisprudence of the Boards of Appeal it is necessary, in order to assess inventive step, to establish the closest state of the art, to determine in the light thereof the technical problem which the invention addresses and successfully solves, and to examine the obviousness of the claimed solution to this problem in view of the state of the art. This "problem-solution approach" ensures the assessment of inventive step on an objective basis.

5.1 Closest prior art

In the context of the problem-solution approach, the Boards of Appeal have developed certain criteria in order to identify the closest prior art. The crucial criteria are that the "closest prior art" is normally a prior art document disclosing subject-matter conceived for the same purpose as the claimed invention and additionally having the most relevant technical features in common.

5.2 The patent-in-suit is concerned with the removal of higher alkyl iodides, more particularly dodecyl iodide, from acetic acid or acetic anhydride (see column 1, lines 5 to 9; column 2, lines 52 to 55).

In relation to this objective and to the relevant technical features in common, a decision must be made as to which of documents (6) and (8) is to be considered as the "closest prior art". The Appellant and the Respondent had divergent views in this respect.

5.2.1 Document (8), which the Appellant considered as the closest prior art, is specifically concerned with the problem of removing iodides from non-aqueous organic media, in particular from acetic acid (see column 1, lines 3 to 12). The specific nature of the iodide compounds to remove is not critical, but they are typically alkyl iodides (column 3, lines 15 to 18; claims 4 and 5), for example, hexyl iodide (Example VIII).

The method for removing the iodide compounds comprises contacting the medium containing said iodide compounds with a macroreticulated, strong-acid, ion exchange resin which has at least one percent of its active sites converted to the silver or mercury form (claim 1). The contact with the resin is operated at a temperature from 17ºC to 100ºC (claim 7). Preferably the resin is of the "RSO3H type" (column 4, line 20), more preferably Amberlyst 15 (column 4, last two lines and Examples).

5.2.2 Document (6), which the Respondent considered as the closest prior art, relates to a process for producing acetic acid by carbonylation of methanol (see column 1, lines 7 to 9). It aims to produce pure carboxylic acid (column 1, lines 16 to 21).

Document (6) identifies only methyl iodide formed by quenching hydrogen iodide with methanol as an alkyl iodide to be removed, the possible presence of other alkyl iodides in the acetic acid produced not being disclosed in that document (see column 7, lines 23 to 47).

The iodide impurities in the acetic acid produced by the process disclosed in document (6) may be removed inter alia by passing the product through one or more ion exchange resin beds, suitable resins including inter alia the macroreticular strong acid cation exchange resin which has at least 1% of its active sites in the silver or mercury form according to the disclosure of document (8) (see column 8, lines 18 to 24).

5.2.3 Thus, neither document (6) nor (8) aims specifically at removing dodecyl iodide from acid acetic.

However, the objective of document (8) of removing any alkyl iodides, for example hexyl iodide, from acetic acid is closer to the objective of the patent-in-suit of removing dodecyl iodide than that of document (6) of removing only those iodide impurities produced in the particular process of preparing acetic acid disclosed in that document, wherein only methyl iodide is specifically identified.

Furthermore, as to the relevant technical features in common, to arrive at the feature of using a macroreticular resin according to step (b) of claim 1 of the patent-in-suit, in document (6) a first choice has to be made to select the method of passing the acid though an ion exchange resin bed (see column 7, line 48 to 53), followed by a second choice to select the macroreticular strong acid cation exchange resin which has at least 1% of its active sites in the silver or mercury form (see column 8, lines 18 to 24), whereas according to the method of document (8) the alkyl iodides are removed by the resin according to claim 1 of the patent-in-suit.

Furthermore, in contrast to document (8), which indicates operating temperatures of from 17ºC to 100ºC (see column 7, lines 37 to 44), document (6) does not disclose any operating conditions for removing the iodides with the macroreticular resin, let alone the temperature at which the acetic acid is contacted with the resin. The temperature is, however, an essential technical feature of the patent-in-suit, claim 1 of the patent-in-suit requiring a temperature of at least 50ºC (main request), from 50ºC to 100ºC (auxiliary request 1) and at least 80ºC (auxiliary requests 2 and 3).

Therefore, document (8) has more technical features in common with the patent-in-suit than document (6).

5.2.4 The Board concludes therefore that document (8) represents prior art which is closer to the invention of the patent-in-suit than document (6).

5.2.5 According to the Respondent document (6) was cited in the patent-in-suit as the starting point for the invention, and additionally for this reason should be taken as the closest prior art.

In paragraph [0009] of the patent-in-suit, the technical problem is formulated with respect to prior art methods using resin beds described in the preceding paragraphs of the patent-in-suit which did not efficiently remove higher organic iodides from acetic acid. Those prior documents describing these methods are cited in paragraphs [0003] to [0007] and include document (8) (see paragraph [0003], column 1, lines 22 to 35; US 4 615 806 being the US equivalent of document (8)). Document (6) is acknowledged in paragraph [0008] of the patent-in-suit without, however, any reference being made to methods of removing iodides with resin beds. Accordingly, if anything, document (8) is cited as a starting point for the invention of the patent-in-suit rather than document (6).

Notwithstanding this finding, a prior art document described in a patent as the starting point for the invention is to be taken as the starting point in the problem/solution approach only if there is no prior art of greater technical relevance to the solution as claimed (see T 800/91, point 6 of the reasons, not published in OJ EPO). This is not so in the present case, since document (8) is much closer to the claimed invention than document (6) (see point 5.2.3 above).

5.2.6 The Respondent further argued that document (6) should be regarded as representing the closest prior art since the acetic acid product stream obtained by the process disclosed in that document contained higher alkyl iodides.

According to the jurisprudence of the Boards of Appeal, the disclosure of a particular prior art document must always be considered as it stands. In the present case, as conceded by the Respondent, document (6) does not disclose that the produced acetic acid contains higher alkyl iodides. Hence, the technical feature relating to the presence of higher alkyl iodides in the acetic acid produced according to document (6), on which the Respondent relies to argue that document (6) is closer than document (8), is not disclosed in that document, with the consequence that this argument does not convince the Board.

5.2.7 According to the Respondent, the choice of document (8) as the closest prior art was based on hindsight, because the present invention was based on the recognition that the acetic acid stream produced by the process of document (6) contained higher alkyl iodides. However, that argument is also irrelevant since claim 1 does not comprise any feature specifying how the acetic acid containing the higher alkyl iodides is obtained, in particular it does not require that it is obtained by a process according to document (6). Thus, the skilled person did not need to "recognise" that the acetic acid stream produced by the process of document (6) contained higher alkyl iodides.

5.2.8 Finally the Respondent submitted that in the case where document (8) was considered to be closer to the invention than document (6), then documents (7) and (10) must be considered to be even closer since these documents disclosed methods for removing C10 alkyl iodide, which was an alkyl iodide structurally closer to dodecyl iodide than the hexyl iodide disclosed in document (8). Furthermore, the methods of removing alkyl iodides were disclosed in these documents as being more efficient than the method according to document (8).

Documents (7) and (10) aim to remove iodides, e.g. C1 to C10 alkyl iodides, from acetic acid (see document (7), claims 1 and 10; document (10), page 2, lines 35 to 37). Accordingly, although mentioning inter alia C10 alkyl iodides, the objectives of these documents principally do not differ from those of document (8) indicating any alkyl iodide and specifying that the specific nature of the iodide compounds is not critical (see column 3, lines 15 to 18).

However, since the methods of documents (7) and (10) principally operate with mesoporous or macroporous resins (see document (7), page 2, lines 29 and 30; document (10), page 2, lines 23 to 26 and 45 to 46) to remove the iodide compounds, the method disclosed in document (8) operating specifically with the macroreticular resins as defined in claim 1 of the patent-in-suit has more technical features in common with the claimed method.

With respect to the argument regarding the lower effectiveness of the method described in document (8) compared to those of documents (7) and (10), the Board notes that Article 56 EPC requires the assessment of inventive step to be made "having regard to the state of the art", Article 54(2) EPC defining the state of the art "to comprise everything made available to the public". As a consequence, there is no legal basis in the EPC to preclude a particular state of the art, in the present case document (8), from being taken into account when assessing inventive step, merely because later published documents, e.g. documents (7) and (10) mention some drawbacks in the method according to document (8), all the more so because the patent-in-suit does not aim to solve these drawbacks.

5.2.9 The Board is therefore of the opinion that document (8) represents the prior art closest to the patent-in-suit.

5.3 In view of document (8), the problem underlying the patent-in-suit, as submitted by the Respondent during the oral proceedings before the Board, is to provide a method of removal of higher alkyl iodides.

5.4 The proposed solution is the method of claim 1 characterized by removing dodecyl iodide by providing a stream of acetic acid or acetic anhydride comprising organic iodides wherein at least 20% of the organic iodides in the stream comprise C10 or higher organic iodides and wherein the organic iodide comprises dodecyl iodide and contacting said stream with the resin at a temperature of at least 50ºC.

5.5 The Board is satisfied that the problem underlying the patent in suit has been successfully solved by the method of claim 1. Moreover, the Appellant did not challenge this finding.

5.6 Finally, it remains to decide whether or not the proposed solution to the objective problem underlying the patent-in-suit is obvious in view of the state of the art.

5.6.1 Document (8) describes removing alkyl iodides from acetic acid with a macroreticulated, strong-acid, ion exchange resin (see point 5.2.1 above). The method is operated at a temperature from 17ºC to 100ºC (see claim 7 and column 7, line 42).

The choice of removing a particular higher alkyl iodide, namely dodecyl iodide, from a stream comprising organic iodides, wherein at least 20% comprise C10 or higher alkyl iodides and comprising dodecyl, together with a particular temperature threshold, namely at least 50ºC, from within the general teaching of document (8) is neither critical nor purposive. This is because no particular effect has been shown to be associated with this choice, which lies within the routine activity of the skilled person faced with the problem of providing an alternative method. This is all the more so, since document (8) explicitly indicates that neither the choice of the iodides to be removed nor the temperature of removal is critical (see column 3, lines 15 to 21 and column 7, lines 37 to 44, respectively).

5.7 Hence, the subject-matter of claim 1 of the patent in suit results from an arbitrary choice within the ambit of document (8) and consequently lacks an inventive step in view of document (8) alone.

5.7.1 The Respondent argued that document (8) did not disclose dodecyl iodide and thus a skilled person would have had no incentive to specifically select this compound.

However, this argument is not convincing since no specific motivation is required to make an arbitrary choice of a particular embodiment from a host of equally possible embodiments in order to provide a mere alternative.

5.7.2 According to the Respondent, dodecyl iodide could not be removed at ambient temperature and therefore the choice of the temperature threshold of at least 50ºC was not arbitrary.

However, in the absence of any substantiating facts and corroborating evidence, the Board considers the Respondent's allegation that dodecyl iodide is not removed at ambient temperature as mere speculation.

Moreover, this allegation is contradicted by the facts. As pointed out by the Appellant, the plot of the isotherm removal of dodecyl iodide at 25ºC in Figure 4, filed with letter dated 1 October 2002 before the Examining Division, clearly shows that dodecyl iodide is removed at 25ºC. Figure 4 is a plot of various elution isotherms at 25ºC, 50ºC, 75ºC and 100ºC showing the concentration of dodecyl iodide in acetic acid over time varying from one to twenty hours and the isotherm at 25ºC of hexyl iodide. Although not specified, the initial dodecyl iodide content in the acetic acid must have been more than 100,000 ppb, since after 20 hours isotherm, i.e. when the resin becomes less efficient, the stream contains that amount of dodecyl iodide. However, at the beginning of the isotherm, i.e. after one hour, the stream contains only 10,000 ppb dodecyl iodide, corresponding to more than 90% dodecyl iodide removal at ambient temperature.

5.7.3 The Respondent further argued that there was no motivation to select a temperature greater than 50ºC since the process of document (8) was preferably carried out at ambient temperature. Furthermore Figure 4 filed with the letter dated 1 October 2002 showed an unexpected level of removal of dodecyl iodide at higher temperatures.

However, Figure 4 fails to indicate the initial concentrations of hexyl and dodecyl iodides in the acetic acid with the consequence that Figure 4 cannot provide a fair comparison, neither for the relative removal of hexyl iodide compared to that of dodecyl iodide, nor for the relative removal of dodecyl iodide at different isotherms.

Irrespective of the fact that Figure 4 does not properly support the effect of higher levels of removal of dodecyl iodide at higher temperatures, that effect is nevertheless obvious in view of document (1), which teaches that it is desirable to operate at a temperature as high as possible in order to effect maximum removal of iodides (see document (1), column 3, lines 49 to 51).

5.8 As a result, the Respondent's main request is not allowable as the subject-matter of claim 1 thereof lacks inventive step pursuant to Article 56 EPC.

Auxiliary request 1

6. Amendments (Article 123(2) and (3) EPC)

Claim 1 of auxiliary request 1 differs from claim 1 of the main request exclusively by the indication of the upper temperature limit of 100ºC for the contacting step (b), said temperature finding support at page 3, line 26 of the application as filed. The requirements of Article 123(2) and (3) are therefore satisfied.

7. Inventive step (Article 56 EPC)

Document (8) already teaches that the temperature at which the removal of iodide compounds takes place is usually from 17ºC to 100ºC (see column 7, line 42). Therefore the indication of the upper temperature of 100ºC in claim 1 cannot render the claimed method non-obvious over document (8).

In these circumstances, the Respondent's auxiliary request 1 is rejected for lack of inventive step.

Auxiliary requests 2 and 3

8. Independent claim 1 of auxiliary request 3 is directed to an embodiment comprised within claim 1 according to auxiliary request 2, namely to the embodiment of a method of removing dodecyl iodide, wherein at least 20% of the organic iodides in the stream comprise higher organic iodides having greater than C10 and wherein the ion exchange resin is a sulfonic acid functionalised resin.

In case this embodiment according to auxiliary request 3 lacked inventive step, a consequence must be that the subject-matter of auxiliary request 2, which comprises that obvious embodiment, cannot, at least to that extent, involve an inventive step either. For this reason, it is appropriate that the subject-matter of claim 1 of the auxiliary request 2 insofar as it relates to the embodiment comprised in claim 1 of auxiliary request 3, and that of claim 1 of auxiliary request 3, is examined first as to its inventive ingenuity.

9. Amendments (Article 123(2) and (3) EPC)

Claim 1 of auxiliary request 2 is based on the combination of original claims 10 and 14, which are identical to granted claims 13 and 17 respectively, wherein the organic iodide comprises dodecyl iodide according to page 3, line 7 of the application as filed.

Claim 1 of auxiliary request 3 differs from claim 1 of the main request exclusively in that step (b) requires a contact temperature with the resin of at least 80ºC instead of at least 50ºC. This amendment, which constitutes a restriction of the claimed scope, is based on original claim 14.

The requirements of Article 123(2) and (3) EPC are thus satisfied.

10. Inventive step (Article 56 EPC)

The considerations concerning inventive step with respect to the main request are neither based on nor affected by the indication of a temperature threshold which is within the teaching of document (8) (see points 5.6.1 and 5.7.2 and 5.7.3 above). As document (8) discloses that the usual operating temperature is up to 100ºC (see column 7, line 42), the indication in claim 1 of the threshold of at least 80ºC cannot render the claimed method non-obvious over document (8).

Thus, the subject-matter of claim 1 of auxiliary request 3, and consequently that of claim 1 of auxiliary request 2, lack an inventive step (Article 56 EPC).