Application of George W. Polly, Jr

331 F.2d 628, 51 C.C.P.A. 1278
CourtCourt of Customs and Patent Appeals
DecidedMay 14, 1964
DocketPatent Appeal 7133
StatusPublished

This text of 331 F.2d 628 (Application of George W. Polly, Jr) 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
Application of George W. Polly, Jr, 331 F.2d 628, 51 C.C.P.A. 1278 (ccpa 1964).

Opinion

RICH, Judge.

This appeal is from the decision of the Patent Office Board of Appeals which affirmed the rejection of claims 1-14 in application serial No. 762,931, filed September 24, 1958, entitled “Modified Poly-oxymethylene.” No claims are allowed.

The invention relates to stabilized poly-oxymethylene and is thus described in appellant’s specification:

“Polyoxymethylene polymers, having recurring • — CH20— units have been known for many years. They may be prepared by the polymerization of anhydrous formaldehyde or by the polymerization of trioxane which is a cyclic trimer of formaldehyde. Polyoxymethylene varies in thermal stability and in molecular weight, depending on its method of preparation.
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“Although polyoxymethylenes prepared by some methods are much more stable against thermal degradation than those prepared by other methods, it is nevertheless desirable for many uses that the thermal stability be increased.
*629 “It has been found in accordance with this invention that polyoxy-methylenes may be stabilized against thermal degradation by reaction with isocyanates and preferably with compounds containing two or more isocyanate groups. [Emphasis ours.]
* * * * * *
“The isocyanate which may be used in accordance with this invention may be either aliphatic or cyclic. Compounds containing two or more isocyanate groups are preferred. Among the specific isocyanate compounds which may be used are aromatic diisocyanates * * *, aromatic monoisocyanates * * *, aliphatic monoisocyanates * * *, aliphatic diisocyanates * * * and triisocyanates * * *.
“The reaction is carried out in a system wherein the isocyanate and the polyoxymethylene are in intimate admixture. The polyoxymethylene may be in the form of finely divided solid particles, as in a slurry, but for best results the polyoxymethylene and the isocyanates are dissolved in a common solvent. * * *
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“The temperature of the reaction is suitably at least about 20 °C. and preferably from about 140° to about 180°C.

Appellant’s examples disclose comparative tests in which samples of both untreated polyoxymethylene and polyoxy-methylene treated with isocyanate are subjected to temperatures conventional for molding operations. Decomposition rate data show greater thermal stability for the treated material.

Claims 1-4 are drawn to composition, 5-14 to method. Claims 1, 4, 5 and 6 are representative :

“1. The reaction product of normally solid resinous polyoxymethyl-ene with an isocyanate.
“4. High molecular weight poly-oxymethylene, having an inherent viscosity of at least 1.0, measured at 60°C. in a 0.1% solution in p-chlorophenol containing 2% alpha pinene, said polyoxymethylene being thermally stabilized by combination with from about 0.1 to about 10 weight percent of a diisoeyanate, based on the weight of the polyoxy-methylene.
“5. Method for improving the thermal stability of polyoxymethyl-ene which comprises reacting said polyoxymethylene with an isocya-nate.
“6. Method for improving the thermal stability of polyoxymethyl-ene, having an inherent viscosity of at least 1.0, measured at 60°C. in a 0.1% solution in p-chlorophenol containing 2% alpha pinene and which loses less than 5.0% in weight per minute when maintained at 222° C in a circulating air oven, which comprises reacting said polyoxymethyl-ene with a compound consisting essentially of an isocyanate.”

The following prior art is relied on:

DuPont British Patent 557,873 Dec. 9, 1943

DuPont British Patent 748,856 May 9, 1956

British 557,873 (hereinafter ’873) deals with a process for making formaldehyde polymer by mixing formaldehyde monomer with isocyanate and aliphatic acyl ketene. 1 After mixing the constitu- *630 exits in any order at below -20 °C., a polymerization is effected under pressure at a temperature of -20° to + 30°C. In reciting the objects of the invention the patent states:

“Another object is the preparation of high molecular weight polymers of formaldehyde of reduced brittleness, little or no tendency to decom-poke at their melting points, and of good flow characteristics at mould-ing temperatures. A still further object is the preparation of tough, unusually stable, polymers of formaldehyde.” [Emphasis ours.]

The patent further says:

“The resultant polymer melts in the 165-175 °C. range. It shows a greater thermal stability than formaldehyde polymers prepared in the absence of isocyanates and aliphatic acylethenone, decomposing only slowly up to 200 °C., whereas formaldehyde polymers prepared similarly but without the aliphatic acyl ketene, as hereinbefore defined, and isocya-nate decompose rapidly even at temperatures as low as 175°C.” [Emphasis ours.]

The quantity of isocyanate and ketene used depends upon their molecular weights, the patent stating:

“The isocyanate or isothiocyanate is used in relatively small amounts between 0.01-2.0 mole per cent, of the formaldehyde employed. The exact amount of isocyanate is dependent upon its molecular weight, 2 — 4 iso-cyanate groups to each thousand formaldehyde molecules generally being most effective.”

The function of isocyanate in the polymerization process is said to be as follows :

“Although the exact manner in which these modifying agents [iso-cyanates and ketenes] function is not known, it is believed that one or both of these modifying agents facilitate the formation of stable, high molecular weight formaldehyde polymers both by removing impurities and by reacting with the terminal methylol groups of the polymer.” [Emphasis ours.]

British 748,856 (hereinafter ’856 > deals with stabilizing formaldehyde polymers

“ * * * by incorporating certain stabilizing agents therein, namely:
“(a) hydrazines, substituted hy-drazines or hydrazides,
“(b) secondary or tertiary monomeric aromatic amines,
“(c) phenols or substituted phenols, or
“(d) ureas, thioureas and their-substitution products.
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“The stabilizing agent is added in an amount of not more than 10% of the weight of the polymer, a preferred range being from 0.1% to. 5%. It can be incorporated in the-polymer in various ways: it may be-introduced during or after the formation of the formaldehyde polymer, in the form of a solution in a suitable solvent or be milled into the polymer.” [Emphasis ours.]

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331 F.2d 628, 51 C.C.P.A. 1278, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-george-w-polly-jr-ccpa-1964.