In re Plumb

470 F.2d 1403, 176 U.S.P.Q. (BNA) 323, 1973 CCPA LEXIS 435
CourtCourt of Customs and Patent Appeals
DecidedJanuary 26, 1973
DocketPatent Appeal No. 8781
StatusPublished

This text of 470 F.2d 1403 (In re Plumb) is published on Counsel Stack Legal Research, covering Court of Customs and Patent Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Plumb, 470 F.2d 1403, 176 U.S.P.Q. (BNA) 323, 1973 CCPA LEXIS 435 (ccpa 1973).

Opinion

BALDWIN, Judge.

This appeal is from the decision of the Patent Office Board of Appeals, adhered to on reconsideration, sustaining the examiner’s rejection of claim 11 of appellant’s application,1 on the basis of certain prior art.

The Invention

Appellant’s invention relates to polyurethane foams, made from polyisoey-anates and polyols, in which polyols derived from polyester or polyester resins, which have normally been used, are partially or totally replaced by “an alkylene oxide adduct of a substantially aliphat[1404]*1404ic-hydrocarbon-insoluble pine wood resin.” It appears from the record that prior to the present invention appellant’s assignee had used aliphatic-hydrocarbon-insoluble pine wood resin, which is relatively low in cost, to replace part of the relatively expensive polyester or poly-ether resins generally used in the reaction. According to appellant’s specification, however,

[s]uch naturally occurring wood resins, which contain carboxyl and phenolic hydroxyl groups, suffer from the disadvantage * * * that the car-boxyl and phenolic hydroxyl groups are considerably less reactive than the hydroxyl groups of the polyether and polyester resins generally used in the polyurethane reaction mixture. Due to this lack of reactivity, it is extremely difficult to react these car-boxyl and phenolic hydroxyl groups of the wood resins with the isocyanate groups within the short period of time encountered in the actual foaming operation. * * * Accordingly, due to this lack of reactivity of the carboxyl and phenolic hydroxyl groups, it is not practical to use these naturally occurring wood resins to wholly or partially replace the polyol in the resin pre-mix portion of the reaction mixture, or to use a substantial amount of the wood resin in the preparation of urethane foams by the one-shot technique.

Appellant subjects the aliphatic-hydrocarbon-insoluble wood resin to an “oxy-alkylation” reaction, and uses the reaction product to replace the generally used polyester and polyether resins. The specification compares the reaction product with unmodified pine wood resin as follows:

The oxyalkylated pine wood resin is more reactive and readily reacts with isocyanate groups to form urethane polymers within a relatively short period of time. As a result, the oxy-alkylated pine wood resin, which is substantially lower in cost than poly-ether and polyester resins, may be used as the sole polyol component in the production of polyurethane foam by both the semi-prepolymer and one-shot techniques.

The specification also states:

Ethylene oxide, propylene oxide and epichlorohydrin are generally preferred as the alkylene oxide which is reacted with the aliphatic [-] hydrocarbon-insoluble pine wood resin to form the oxyalkylated resin, for these oxides are readily available commercially and form an oxyalkylated resin which has a handleable viscosity when heated to about 300°F. Other alkylene oxides capable of oxyalkylating the pine wood resin may, of course, be used provided that the resulting oxy-alkylated pine wood resin, upon being heated to temperatures of about 300 °F, has a viscosity such that the resin may be pumped and mixed. Claim 11, the sole claim remaining in

the case, reads as follows:

11. A polyurethane foam comprising the reaction product of an organic polyisocyanate and a polyol containing a plurality of hydroxyl groups, in the presence of a blowing agent, wherein up to 100% of said polyol is an alky-lene oxide 2 adduct of a substantially aliphatic-hydrocarbon-insoluble pine wood resin.

The Rejection

The prior art relied on by the examiner is a patent to Delmonte.3 Delmonte discloses polyurethane foams in which the polyol component is a mixture of [1405]*1405conventional polyols and an oxyalkylated petroleum-hydrocarbon-insoluble pine wood resin. The resin is oxyalkylated by reaction with either ethylene oxide or propylene oxide. The sole question before us is whether a showing made by appellants under Patent Office Rule 131 is sufficient to antedate the Delmonte reference.

The Rule 131 showing included two affidavits by appellant Plumb, an affidavit by one Walter E. Voisinet, who was apparently appellant’s immediate supervisor at the time of invention, and a number of documentary exhibits. Exhibit A is a letter from Plumb to Voisi-net entitled “Attempted Oxyalkylation of Vinsol.” Vinsol is identified in appellant’s specification as an aliphatic-hydrocarbon-insoluble pine wood resin. Exhibit A describes the reaction of Vin-sol with epichlorohydrin and the use of the resulting adduct in the preparation of a foam. That foam is compared with another foam, whose composition was the same, except the latter foam was made with Vinsol which had not been reacted with epichlorohydrin. Exhibit B is a memorandum of invention entitled “Oxyalkylation of Vinsol.” The text of the memorandum reads as follows:

Vinsol is a resin derived from Southern Pine Wood, having an [sic] reactivity No. of from 84 (By NCO Acid Nos.) to 284 (By Zerewitinoff Method). It is known that these Hydroxyl groups are principally phenolic in character. Phenolic novolacs have been oxyalkylated commercially for several years.

We propose as an invention, the oxy-alkylation of vinsol (either or both of the Hydroxyl and Carboxyl groups). The oxyalkylation may be accomplished through the use of agents such as ethylene oxide, propylene oxide or epichlorohydrin. We also propose to aminate vinsol with agents such as ethylene imine to give products reactive to isocyanates.

Exhibit C is another letter from Plumb to Voisinet, which describes the reaction of Vinsol with epichlorohydrin. Exhibits D through 0 are copies of notebook pages dealing with the experiments described in Exhibit A. The dates of Exhibits A through 0 are all alleged to be prior to the critical date. Exhibit P is a copy of “The Carwin Company Technical Bulletin,” dated April, 1962. Exhibit P was cited to “show a small portion of what was well known in the period prior to December 31, 1963 [the filing date of the Delmonte patent].”

One of the Plumb affidavits states:

The facts surrounding my conception and reduction to practice are the following. My employment with National Gypsum Company started in 1962, and from the start of said employment throughout the period ending December 31, 1963, I was employed almost solely in research and development related to rigid polyurethane foam. Prior to the start of my said employment, National Gypsum Company had commenced using an ali-phatie-hydroearbon-insoluble pine wood resin, commonly known as Vin-sol, in substantially all of the regular production of its rigid polyurethane foam.

The Plumb affidavits describe the Exhibits, stating the following about appellant’s memorandum of invention:

This Exhibit B sets forth my recognition at that time of the oxyalkylation of Vinsol with ethylene oxide, propylene oxide or epichlorohydrin. From the other documents submitted it can be seen that my work regarding the oxyalkylation of Vinsol, as referred to in Exhibit B, was a first step in the preparation of polyurethane foam, and I can herein state that this concept in Exhibit B was solely related to preparation of polyurethane foam.

The Voisinet affidavit states that “from the said start of employment until December 31, 1963, said Dr.

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Bluebook (online)
470 F.2d 1403, 176 U.S.P.Q. (BNA) 323, 1973 CCPA LEXIS 435, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-plumb-ccpa-1973.