T 0172/95 05-03-1998

1. The appeal is admissible.

Sufficiency of disclosure

2. An invention is sufficiently disclosed when a skilled person can carry it out on the basis of the information provided by the patent specification in the light of common general knowledge.

2.1. It is generally accepted that "a person skilled in the art", is presumed to be an ordinary practitioner or a team of ordinary practitioners, aware of what was common general knowledge in the art at the relevant date, capable of following instructions, but not having any inventive capability (see T 39/93, OJ EPO 1997, 134, Reasons for the Decision, point 7.8.4), who is capable of recognising and rectifying errors in the description (T 171/84, OJ EPO 1986, 95 and T 226/85, OJ EPO 1988, 336). In the present case it means that the skilled person is an ordinary polymer chemist or a team of ordinary polymer chemists familiar with the various problems encountered when producing polymers, in this case polyethylene, and knowledgeable about the standard methods used to analyse the products, who would know which analysing and calculation methods would not be correct. In view of the Appellant's objections concerning (i) the fractionation method, in particular the cooling step and (ii) the calculation methods for parameters (C), (D), (E) and (F), first the skilled person's common general knowledge on those two points has to be established and secondly, the information provided in the patent in suit, in the light of that common general knowledge, has to be analysed. Also, as the Appellant's arguments boil down to the assertion that the methods used in the patent in suit were incorrect and would not be applied to the category of copolymers with which the patent is concerned, it has to be established whether, based upon his common general knowledge and the information contained in the patent specification, the skilled person would have been inclined not to follow the instructions in the patent specification.

2.2. Regarding the fractionation method, several documents filed by the Appellant on 12 July 1995, during the written proceedings before the Board:

B: Bull. Soc. Chim. Belg., vol. 59, 1950, 476-489 (in particular 477: II. Technique opératoire),

C: J. Pol. Sc. Part A, vol. 3, 1965, 907-916 (in particular 909 to 913) and

D: J. Pol. Sc.: Pol. Phys. Ed., vol. 20, 1982, 441-455 (in particular 442),

show that the method according to which the polymer is first coated upon a support and then eluted by stepwise raising the temperature of the eluent and completely dissolving the polymer at every particular temperature, called preparative-scale temperature elution fractionation (hereinafter P-TREF), belonged to the state of the art and was a well-known analytical method for polymers at the priority and filing dates of the patent in suit. Document C (in particular Figures 4 and 5) also shows the fractionation and refractionation results of samples of polymer, which demonstrate the heterogeneous character not only of the polymer itself, but also of its fractions. Also comparisons of the theoretical values with the actually measured values are made. The differences between P-TREF and the later developed continuous analytical-scale temperature rising elusion and fractionation (hereinafter A-TREF) are also described in document D. In the light of those documents there can be no doubt that the skilled person was familiar with the P-TREF method and the differences between P-TREF and A-TREF and that he would know that the polymer fractions in themselves were not homogeneous but, like the polymer itself, for their part also contained a distribution of short chain branching degrees. Therefore, the Board considers this knowledge as belonging to the general common knowledge of a person skilled in the field of polyethylene polymers.

2.3. The patent specification contains the following information about the fractionation method (page 4, lines 29 to 44):

"The copolymer (10 g) is added to about 2 liters of a mixture of p-xylene and butyl Cellosolve® (80:20 by volume) and the mixture is heated at about 130 C in the presence of 2,5-di-tert.butyl-4-methylphenol (0.1% by weight based on copolymer) as a heat stabilizer. Then, about 1 kg of diatomaceous earth (tradename Celite® #560, made by Johns-Manville Company, U.S.A.) is added to the resulting solution, and the mixture is cooled to room temperature with stirring. This operation results in coating the copolymer on diatomaceous earth. Then, the entire mixture is filled in a jacketed cylindrical column (diameter about 3 cm) which is set perpendicularly. While the column is maintained at a temperature of 30 C, a solvent having the same composition as the above mixed solvent in the same volume as a solution flowing from the bottom of the column is passed (about 1 liter/hr) through the column from its top. The solution flowing out from the bottom of the column is collected in a receiver. To the collected solution is added methanol in an amount twice the volume of the collected solution to precipitate the eluted copolymer. After confirming that upon addition of methanol, the copolymer no longer precipitates, the flowing of the solution is stopped. The temperature of the column is then raised to 35 C, and the flowing of the solution and the passing of the mixed solvent are resumed and continued until the copolymer no longer flows out. The foregoing operation is carried out at intervals of 5 C until the operation is finally carried out at 120 C. The copolymer fractions precipitated from methanol are separated by filtration and dried to obtain fractions."

2.3.1. From that passage it is clear that elution is carried out stepwise and not gradually (page 4, lines 38 to 42: "until the copolymer no longer flows out"), which supports the Respondent's argument that the method used is P-TREF, not A-TREF. On the basis of his common general knowledge (see point 2.2 above), the skilled person would thus be well aware of the fractionation method to be used for the determination of the parameters (C), (D) and (E).

2.3.2. As the Appellant stated, the passage does not contain any indication about the cooling rate during the first step. The Appellant argued that different cooling rates led to different results in the second step, which argument was supported by a direct reference to Figures 3 and 4 of document A.

Those figures show the distribution of TREF-fractions as a function of elution temperature for different cooling rates and it cannot be denied they are different. That does however not mean that the parameters defining the presently claimed polymer are also different or that differences in the elution patterns automatically result in different values of those parameters. The Appellant brought no proof that such would be the case.

The Respondent, however, did support its statement that the results obtained with P-TREF were substantially independent of the cooling rate in the first step, by submitting plots which show the relationship between the cumulative weight fraction and the composition distribution parameter (U) calculated from the data of Figures 3 and 4 of document A (statement of 19 March 1996, page 4, second complete paragraph and annex).

In the light of this evidence, the Board considers that the Appellant's argument that the cooling rate influences the results of the fractionation method in such a way as to change the values of the parameters now being claimed, is not sufficiently supported by evidence. Therefore, the Appellant's argument cannot be accepted.

2.4. According to the patent specification, the values of parameters (C), (D) and (E) are calculated as follows:

"The weight of each of the fractions is then measured, and the degree of branching per 1000 carbons [C] of each of the fractions is determined by the 13C-NMR method shown below with regard to the characteristic (D). Since the degree of branching per 1000 carbons [C] of the fraction decreases as the eluting temperature rises, the cumulative weight fractions [I(w)] are calculated in the decreasing order of the eluting temperature. Under the assumption that the number of branches per 1000 carbons [C] and the cumulative weight fraction [I(w)] in each fractionated portion follow the integral function of the logarithmic normal distribution (emphasis added), which is the following equation (2), parameters and C0 equation (2) are determined by using the method of least square.

FORMULA

(The amendment by the Board of 2 into 2 involves the correction of an obvious typing error.)

and C0 are given by the following equations. FORMULA

Thus, Cn and Cw can be easily calculated." (page 4, lines 45 to 65)

and:

"The degree of branching, as used herein, denotes the number of branches per 1000 carbons in the copolymer chain, and is determined in accordance with the method disclosed in G. J. Ray, P. E. Johnson and J. R. Knox, Macromolecules, l0, 773 (1977) from the area intensity of a signal of methylenic carbon adjacent to a branch observed by the 13C-NMR spectrum. For example, when the comonomers of a copolymer are butene-1 and 4-methylpentene-1, the positions of the chemical shifts of the signals assigned to the above methylenic carbons are respectively 33.8 ppm and 34.5 ppm with TMS (tetramethylsilane) as a standard." (page 5, lines 12 to 18)

and:

"The amounts of components having not more than 2. branches/1000 carbons and components having at least 30. branches/1000 carbons are determined as follows: __ The relation between the cumulative weight fractions and the degrees of branching obtained from the fractionation of the copolymer performed in determining U with regard to the characteristic (C) is plotted on a graph, and the points corresponding to two branches/1000 C and 30 branches/1000 C on the graph are interpolated. The cumulative weight fractions corresponding to these points are determined based on the results, and the above amounts can thus be determined." (page 5, lines 29 to 35).

2.4.1. From that information it is clear that the weight of each of the fractions is measured and that the degree of branching is determined by 13C-NMR according to well-known methods and there can be no doubt that the skilled person would have known how to apply them and indeed would apply them. This means that the patent specification provides a clear teaching about how to perform a reliable measurement of the degree of short chain branching in the copolymer chain.

2.4.2. As indicated on page 4, lines 52 to 65 of the patent specification, the calculation methods for the parameters (C), (D) and (E) rely on the assumption that the number of branches per 1000 C-atoms and the cumulative weight fraction I(w) in each fractionated portion follow the integral function of the logarithmic normal distribution. This provides a clear instruction to the skilled person not to depart from that assumption.

Although the Appellant stated that that assumption for most polymers was wrong and would lead to erroneous and unreliable results, it failed to provide any proof that such was indeed the case and that the results of calculations based upon the assumption would not be reproducible. As the Board can see no reason why the results obtained according to the teaching of the patent in suit would not be reproducible, it is satisfied that, even if the above-mentioned assumption would not be correct from a theoretical point of view, the instruction is so clear and unambiguous that the skilled person would know how to apply it and indeed would apply it and obtain reproducible results.

2.4.3. As pointed out above (point 2.2), the skilled person knew that the fractions obtained by P-TREF were heterogeneous, or, in other words, that they did not contain one kind of polymer molecule with one, precisely defined, degree of short chain branching, but instead a mixture of polymer molecules having different degrees of short chain branching and that such a fraction, when measured, presented an average degree of short chain branching corresponding to its specific mixture of polymer molecules. In the light of that knowledge, the indication in the patent specification that the distribution of polymer molecules in each fractionated portion is assumed to follow the integral function of a logarithmic normal curve and that the calculations of the short chain branching are based upon that assumption (page 4, lines 50 to 52), cannot be misunderstood and the skilled person would carry out the calculation accordingly.

2.4.4. Regarding the parameters (D) and (E) the additional information that the points corresponding to 2 and 30 branches respectively, should be interpolated (page 5, lines 29 to 33), is self-evident, since one would not expect the actual measured values of the fractions to be exactly 2 and exactly 30 branches per 1000 C-atoms, which are the basis for the definition of those parameters. Therefore, that passage does not render the instructions unclear, on the contrary, it merely reflects common general knowledge.

2.4.5. The objection against the calculation method of parameter (F) was raised for the first time only in the Statement of Grounds of the Appeal and the Respondent requested that it be ignored. The lateness of the objection in itself can, however, not be a bar to consideration by the Board, as it concerns not a new ground, nor new evidence or a new fact, but a new argument, which could be dealt with even in the absence of the other party (G 0004/92, OJ EPO 1994, 149).

The patent in suit gives the following information regarding the measurement of parameter (F):

"In the present invention, the above ratio in characteristic (F) is determined from the average methylene chain length calculated by using 13C-NMR and the average block methylene chain length calculated by excluding the case where the number of methylene groups between two adjacent branches is not more than 6, and defined as the ratio of the average block methylene chain length to the average methylene chain length. The block methylene chain length is the number of methylene groups between branches determined from the signals of the third and fourth and subsequent methylenic carbons observed when the number of methylene groups between branches is at least 7. The positions of the chemical shifts of the signals assigned to the third and fourth and subsequent methylenes are 30.1 ppm and 29.6 ppm, respectively, with TMS as a standard." (page 5, lines 52 to 59).

In the Board's opinion, those instructions are clear enough for the skilled person to carry them out. The Appellant's written argument (Statement of Grounds of Appeal, page 7, second complete paragraph) did not go beyond the mere observation that the definition was not well-defined and during the oral proceeding the issue was not further substantiated, so that it is not clear how that objection should be understood. Therefore, the Board cannot accept the Appellant's argument.

2.5. For the above reasons, the Board concludes that the patent specification contains sufficient information regarding the measurement and calculating methods of the various parameters defining the claimed polymer for the skilled person to carry them out. Furthermore, in the Board's view, the skilled person would, on the basis of that information, in the light of his common general knowledge, not deviate from it, so that the requirements of Article 83 EPC are fulfilled.

Priority

3. The Appellant's objections concerned the fractionation method, the calculation methods for parameters (D) and (E) and the number of melting points, which were different in the priority document and in the patent in suit (Statement of Grounds of Appeal, page 1, fourth paragraph).

3.1. Regarding the fractionation method, the English translation of the priority document reads:

"For carrying out the fractionation of the ethylene copolymer, it is dissolved in a solvent mixture (volume ratio: 80/20) of p-xylene and butyl Cellosolve in the copresence of 2,5-di-tert-butyl-4-methylphenol as a thermal stabilizer, after which the solution is coated on diatomaceous earth (tradename CELITE #560, a product of Johns-Manville Company, U.S.A.). The coated diatomaceous earth is then packed in a cylindrical column. While causing the passage and flow through the column of a solvent having the same composition as that described above, the temperature inside the column is raised from 30 C to 120 C stepwise at 5 C graduations to fractionate the ethylene copolymer. This is followed by reprecipitation in methanol, separation by filtration and drying to give the fractions." (page 12, last paragraph to page 13 line 7).

Compared with the text of the patent in suit, a number of differences are present, of which the amounts of polymer and solvent, the temperature at which the polymer is solved and the cooling while stirring are the most important ones as they might influence the fractionation results. The other differences are mostly of editorial nature. Although the Appellant argued that the effect of those differences would result in different polymers being claimed in the priority document and in the patent in suit, no evidence whatsoever in support of that contention was provided. In particular, it has not been shown that any changes in the conditions of the first step of the P-TREF method would lead to modifications in the values of the parameters defining the claimed polymers. By contrast, as was the case with the sufficiency issue (point 2.3 above), the Respondent did provide evidence of the contrary. Therefore, the Appellant's argument has to be rejected.

3.2. Regarding the calculation methods for parameters (C), (D) and (E), the priority document lacks the following passage (page 5, lines 29 to 35 of the patent specification):

"The amounts of components having not more than 2. branches/1000 carbons and components having at least 30. branches/1000 carbons are determined as follows: __ The relation between the cumulative weight fractions and the degrees of branching obtained from the fractionation of the copolymer performed in determining U with regard to the characteristic (C) is plotted on a graph, and the points corresponding to two branches/1000 C and 30 branches/1000 C on the graph are interpolated. The cumulative weight fractions corresponding to these points are determined based on the results, and the above amounts can thus be determined."

As stated above (point 2.4.4), that information does not change anything to the actual method of determination of the parameters (D) and (E), but merely specifies how on that basis a person skilled in the art would normally operate in order to determine the exact amounts of components having not more than 2. branches/1000 carbon atoms and components having at least 30 branches/1000 carbon atoms. Therefore, the introduction of the above passage into the application as filed does not change anything in the definition of the ethylene copolymer, hence does not modify in substance the teaching of the priority document.

3.3. As to the number of melting points, in the priority document the polymer could have one or more melting points (feature (G) in the claim and page 16, last paragraph to page 7, first paragraph), whereas the present claims refer to one or three or more melting points, thus excluding the possibility of two melting points. Although the Appellant during the written proceedings stated that that exclusion changed the character and the nature of the claimed subject-matter (Statement of Grounds of Appeal, page 2, second paragraph), the Appellant did not explain in which way, nor was any evidence provided that the excluded feature was technically essential for achieving the object of the invention. During the oral proceedings the matter was not further argued.

A comparison of the description of both documents shows that the objectives (page 2, lines 5 to 10 of the patent specification; the paragraph bridging pages 3 and 4 of the English translation of the priority document) have remained the same: copolymers having a well-balanced combination of transparency, impact strength, tear strength, blocking resistance, environmental stress cracking resistance, heat resistance and low-temperature heat-sealability for a density of 0.90 or more. For copolymers with a density of less than 0.90, the emphasis lies on transparency, impact strength and low-temperature heat-sealability and the suitability for improving the impact strength and low-temperature heat-sealability of other polymers in which they are incorporated.

No particular mention is made of the number of melting points, but a number of examples present in the priority document have been deleted. As the tables in the priority document do not give the number of melting points of the exemplified polymers, no conclusion regarding that feature can however be drawn from the deletion of some examples. In fact, according to page 18, lines 2 to 11 of the priority document, which corresponds to page 6, lines 16 to 21 of the patent specification, the features which are decisive for the desired balance of properties are not the number of melting points, but, on the one hand, the actual value of T1, and, on the other hand, the differences T1-Tn or T1-T2; thus, in that respect also, the definition of the copolymer in the priority document and in the patent in suit is the same. Therefore, there is no evidence that the number of melting points would play a technical role in the sense of being essential to achieve the invention's objectives. Accordingly, a change of character and nature of the invention as defined in the priority document cannot be recognised.

3.4. In view of the above, the priority of the patent in suit is validly claimed.

Prior art

4. In the light of the valid priority of 21 October 1983 of the patent in suit, D1, which was filed on 25. October 1983 with a priority of 25 October 1982 belongs to the state of the art according to Article 54(3)(4) EPC. According to the Appellant, D2, which claims the same priority as D1, is not entitled to it. The Respondent did not contradict that statement and the Board sees no reason to deviate from those opinions. Therefore, D2 is not considered to be state of the art within the meaning of Article 54(2) or 54(3) EPC. D5 and D10 have been published before the priority date of the patent in suit, so that they form prior art under Article 54(2) EPC.

Novelty

5. The novelty objection was based upon D1, which describes an ethylene copolymer having in combination the following characteristics (A) to (I):

(A) it has a melt flow rate of from 0.01 to 200 g/10 min.;

(B) it has a density of from 0.900 to 0.945 g/cm3;

(C) it has a composition distribution parameter (U), defined by the following equation (1)

U=100 x (Cw/Cn - 1)

wherein Cw is the weight average degree of branching, and Cn is the number average degree of branching, of not more than 50;

(D) the amount of components having a degree of branching of not more than 2/1000 carbons is not more than 15% by weight based on the ethylene copolymer;

(E) the amount of components having a degree of branching of at least 30/1000 carbons is not more than 15% by weight based on the ethylene copolymer;

(F) an average chain length ratio of the methylene groups is not more than 2.0;

(G) it has n melting points measured by a differential scanning calorimeter (DSC) (where n 2); the highest melting point T1 among these DSC melting points is given by the following equation

T1 = (175 x d - 46) 125 C

wherein d is the density (g/cm3) of the copolymer;

the difference between T1 and the lowest melting point Tn among the DSC melting points is given by

0. C < T1 - Tn 18 C;

and the difference between T1 and the second highest melting point T2 is given by the following expression (iii)

0. C < T1 - T2 5 C,

provided that when there are two (n=2) melting points, the difference is in accordance with the above expression

0. C < T1 - Tn 18 C;

(H) the ratio of the amount of heat of crystal fusion H1 at the highest melting point T1 to the total amount of heat of crystal fusion HT is given by the following expression

0. < Hl/HT 0.40; and

(I) it is a copolymer of ethylene with at least one C4-C20 -olefin (Claim 1).

5.1. As can be seen from a comparison with present Claim 1 (point I above), a number of ranges overlap but do not have the same limits, whereas the requirement for T1 - Tn is different over the whole range. Values of above 18. C in D1 can however be found in Comparative Examples 1 and 2 (19.2 and 19.4, respectively); according to page 12, lines 13 to 18, when T1 - Tn is higher than 18 C, the tear strength, impact strength and low-temperature heat-sealability of the copolymer are deteriorated, and it is difficult to provide the desired excellent properties in a well balanced combination (Tables 2 and 3).

5.2. The fact that in Comparative Examples 1 and 2 T1 - Tn falls within the range now required for characteristic (G) does not render them detrimental to novelty, since other parameters, in particular the U-parameter (Comparative Example 1:55 and Comparative Example 2:108), fall outside the scope of the present claims. The Appellant argued that the difference in the values of the U-parameter should be disregarded as it was an unusual one for which no reliable method for determination existed. In reality, as demonstrated above (point 2), the method to determine the value of U is clear and reproducible. Moreover, the U-parameter is based upon standard methods for analysing ethylene copolymers, which were also used in D1, so that it can be accepted as an indicator for differences between polymers. For those reasons, the Appellant's argument must fail.

5.3. Regarding the passage on page 12 of D1, there is no indication whatsoever that the other parameters have values within the present ranges. Not only can the values of the other parameters be outside the scope of the claimed subject-matter as the ranges do not exactly correspond (parameter (B) is 0.900 to 0.945 in D1, 0.850. to 0.930 in the patent in suit; parameter (D) is not more than 15% in D1, not more than 10% in the patent in suit), but also there is no indication that the other parameters retain their indicated values when the value of T1 - Tn is changed. On the contrary, since the catalysts actually used in the examples of D1 and in those of the patent in suit are not prepared in the same way, in view of the complex nature of those catalysts it is highly probable that they do not produce the same polymers. Anyhow, the Appellant, who as the Opponent has the onus of proof, provided no evidence that they do. Therefore, there is no reason to assume that the values of T1 - Tn higher than 18 C mentioned in Comparative Examples 1 and 2, without any reference to the other parameters of the polymer, automatically mean that the latter, too, would fall within the ranges required according to the patent in suit. The disclosures of D2 (which is not prior art) and D10, upon which the Appellant relied to demonstrate the implicit disclosure of the comonomer percentage and parameters (A), (B), (I) and (J) of the polymers of D1, do not change anything in that respect. Accordingly, it is concluded that D1 does not explicitly or implicitly disclose all the combined features of the present polymers.

5.4. No other documents were cited against the novelty of the claimed subject-matter and the Board agrees with that view.

5.5. For those reasons, the subject-matter of Claim 1 as well as that of Claims 2 to 4 is novel.

Admissibility of inventive step objection

6. The Respondent objected to the issue of inventive step based upon D5 being raised in the appeal proceedings, since the Appellant had not provided any arguments as to why D5 would be detrimental to inventive step (statement filed on 19 March 1996, page 6, last paragraph). However, in the Notice of Opposition, to which the Appellant referred for its inventive step objection, in point 5, page 9, second full paragraph, it was argued that the skilled person, in view of a number of other documents, would be encouraged to vary the catalyst system and polymerization conditions of D5 in order to optimize the characteristics of the polymer. Therefore, the issue of inventive step had been raised during the proceedings before the first instance, so that no new ground is introduced at the appeal stage. Also, D5 has been mentioned and used as a support for that objection as from the beginning. Therefore, there are no new facts or evidence. Since in the conclusion of the Statement of Grounds of Appeal the Appellant made an explicit reference to the arguments presented in the Notice of Opposition, it cannot be maintained that new arguments have been introduced in the proceedings before the Board either. Hence, the issue of inventive step is admitted into the proceedings.

Inventive step

7. The patent in suit concerns a linear ethylene copolymer.

7.1. Such copolymers are disclosed in D5, which the Board, like the Opposition Division and the parties, regards as the closest state of the art. D5 (Claim 1) describes a copolymer of ethylene and a minor proportion of an -olefin having 4 to 10 carbon atoms, which has the combined properties of:

(1) a melt flow rate of 0.1 to 100 g/10 min.,

(2) a density of 0.91 to 0.94 g/cm3 and

(3) a xylene absorption per unit amorphous region (Y) satisfying the formula:

Y < _ 0.80 X + 0.67

wherein X is the degree of crystallinity of the copolymer.

Although the copolymer is said to have excellent transparency, impact resistance and opening (blocking) property (column 1, lines 49 to 52; column 2, lines 5 to 11) the low temperature heat-sealability and tear strength were capable of improvement.

7.2. According to the patent specification (page 2, lines 5 to 10), the technical problem underlying the patent in suit is to be seen in providing a polymer that would have an advantageous combination of transparency, impact strength, tear strength, blocking resistance, environmental stress cracking resistance, heat resistance and low-temperature heat-sealability.

7.3. According to the patent in suit this problem is to be solved by an ethylene copolymer having the features as defined in Claim 1.

7.4. The examples and comparisons with the prior art in the patent (Tables 1 to 3) show that only some aspects of the above-defined problem are effectively solved. In particular, it has been shown that films made out of the polymers according to the patent in suit have a favourable combination of transparency, impact strength, tensile strength, blocking properties and low temperature heat-sealability. However, the examples contain no information about the environmental stress cracking resistance and heat resistance, so that it cannot be concluded that the above defined technical problem is effectively solved in respect of those properties.

7.5. Therefore, the technical problem has to be reformulated on a less ambitious basis, namely as to provide a polymer that has an advantageous combination of transparency, impact strength, tear strength, blocking resistance and low-temperature heat-sealability, which problem, as pointed out above (point 7.4), has been effectively solved.

8. The issue to be decided, therefore, is whether the claimed subject-matter is obvious having regard to the documents on file.

8.1. The general teaching of D5 is that ethylene copolymers having a single melting point, hence a uniform distribution of comonomers, are very suitable for producing films having good transparency, tear resistance, impact resistance and blocking property (column 5, lines 5 to 7 and 24 to 31). The importance of polymers having only one melting point is emphasised (column 4, line 67 to column 5, line 13). In that light, it was not to be expected that it would be possible also to produce polymers having three or more melting points that would exhibit an advantageous combination of the above-mentioned properties. Moreover, as D5 is completely silent about low temperature heat-sealability, there would be no incentive on the basis of the teaching thereof to consider the specific combination of features of present Claim 1 in order to arrive at a polymer having not only the above-mentioned favourable combination of properties, but also the additional advantage of low temperature heat-sealability. Therefore, D5 alone does not render obvious the definition of the polymers now being claimed.

8.2. In its Notice of Opposition, the Appellant combined the teaching of D5 with other documents, arguing that the skilled person would have been encouraged to vary the catalyst system and polymerization conditions for reasons of optimization and that each of those documents pointed to homogeneous copolymers. However, none of those documents even remotely refers to the specific combination of features of the present copolymers. Therefore, even if the skilled person would indeed have been encouraged to vary the catalyst, there was no incentive whatsoever to vary it in such a direction as to arrive at the present polymers.

8.3. For those reasons, the Board concludes that the subject-matter of present Claim 1 cannot be derived from the documents relied upon by the Appellant, whether taken alone or in combination, and, therefore, involves an inventive step.

9. As Claim 1 is allowable and Claims 2 to 4 relate to further embodiments, articles made of and use of the polymer according to Claim 1, their patentability is supported by that of Claim 1.

Referral to the Enlarged Board

10. The Respondent's request to refer the case to the Enlarged Board of Appeal has not been maintained during the oral proceedings. Therefore, it needs not be dealt with.

Apportionment of costs

11. The Respondent requested an apportionment of costs for several reasons that encompass a late filed ground of opposition, late filed arguments and an abuse of procedure.

11.1. The ground of insufficient disclosure has been argued from the very beginning of the opposition. The Notice of Opposition, filed on 28 November 1990, explicitly mentions this ground (page 1, second paragraph), so that there can be no question of a late filed ground and an apportionment of cost for this reason has to be refused.

11.2. The ground of insufficient disclosure was based on the description of the polymerisation conditions in D1 and D2 (Notice of Opposition, point 13). No mention was made of any difficulty in applying the calculation methods according to the patent in suit in the Notice of Opposition. Later in the proceedings that difficulty was explained, but only in respect of lack of novelty, not insufficiency. The first time the argument was raised in connection with insufficiency was in the Statement of Grounds of Appeal. Therefore, the Board agrees with the Respondent that the argument was raised at a late stage. However, according to G 0004/92 (supra), the opponent can raise new arguments based on grounds, facts and evidence already present in the proceedings and this can be done even if the other party is absent. In the present case, the argument had been mentioned in writing before and hence it could be referred to later. Therefore, an apportionment of costs based on this reason has to be refused.

11.3. The EPC does not give a binding effect to decisions taken previously by the same or another Board in respect of different cases, even if the issues under discussion are exactly the same. Therefore, the principle of res iudicata does not apply with regard to different cases and, for that reason, there can be no question of abuse if the Appellant raises the same arguments regarding the same points in different cases.

Moreover, in the present case, most of the issues are different from those of T 1113/92 (supra). In particular, the details of the fitting procedure for determining the U-parameter, which was the main issue in decision T 1113/92, have not been disputed in the present case; similarly, other points which had not been addressed in that decision, have been at issue in the present proceedings. Accordingly, the Board does not consider that the Appellant, in exercising its entitlement to opposition and appeal, has committed an abuse of procedure.

11.4. Moreover, from the above considerations it is clear that the costs actually incurred by the Respondent did not go beyond the expenses a patent proprietor can normally expect to have to face when defending his patent in opposition/appeal proceedings. In particular, the issues raised by the Appellant did neither cause the Respondent to carry out additional experimental tests, nor result in additional oral proceedings taking place.

11.5. Therefore, the Board sees no reason to depart from the principle set out in Article 104(1) EPC according to which "Each party to the proceedings shall meet the costs he has incurred...". It follows that the request by the Respondent for an award of costs pursuant to Rule 63 EPC is to be rejected.