Holliday v. Pickhardt

29 F. 853, 24 Blatchf. 201, 1887 U.S. App. LEXIS 2407
CourtU.S. Circuit Court for the District of Southern New York
DecidedJanuary 29, 1887
StatusPublished
Cited by10 cases

This text of 29 F. 853 (Holliday v. Pickhardt) is published on Counsel Stack Legal Research, covering U.S. Circuit Court for the District of Southern New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Holliday v. Pickhardt, 29 F. 853, 24 Blatchf. 201, 1887 U.S. App. LEXIS 2407 (circtsdny 1887).

Opinion

Wallace, J.

This suit- is brought to restrain infringement of letters patent No. 250,247, dated November 29,1881, issued to John Holliday, assignor, etc., and also to vacate letters patent No. 250,201, of the same date, now owned by the defendants, issued to Heinrich Caro, assignor, etc. Both patents claim a chemical product as a new article of manufacture, and the process by which it is produced. The product claimed in each is a coloring matter having specified properties or characteristics, and the process claimed in each relates to the conversion of rosaniline into a sulpho-acid, which is capable of being used in an acid-dye bath, and, when so used, will retain the original rosaniline or magenta color.

The application for the Holliday patent was filed in the patent-office, December 24, 1877, and the application for the Caro patent was filed March 28,1878. Interference between the two applications was declared July 2, 1878, and, after the taking of proofs, priority was awarded, by the primary examiner, to Holliday, February 11, 1881. Subsequent proceedings took place in the patent-office to ascertain, among other things, whether the specimen product filed by Holliday at the time of his application was the dye-stuff in controversy, and whether such dyestuff could be produced by following the process of the Holliday application; and a decision resulted in favor of Holliday. An appeal was taken from the decision'of the primary examiner, by Caro, but this was withdrawn before the decision of the appeal to the commissioner of patents. No material amendment was subsequently made in the Caro application; and the action of the patent-office in issuing a patent to each applicant is denounced by the plaintiff's as unwarranted, and is justified by the defendants upon the hypothesis that the applications were, in fact, for different inventions.

The proofs sustain the findings of the patent-office that Holliday was the prior inventor of the process and product of his patent. They also sustain the decision of the patent-office that a dye-stuff having the properties specified in the Holliday patent can be produced by following the description of the process in the patent.

The primary question in the case is whether the product claim of the Caro patent is for the same now article of manufacture embraced in the product claim of the Holliday patent, and whether the process claim in each patent is for the same invention. The material parts of the Holliday patent are as follow's:

“The coloring matter which I operate upon is known commercially as ‘ rosaniline,’ ‘fuehsine,’ ‘ magenta,’ or ‘aniline red,’ these being classed as aniline reds. It is well known that, owing to the character of rosaniline, the coloring matter thereof cannot be employed, either alone, or mixed with other coloring matters, where the process of dyeing or printing requires the employment of an acid or acid mordant. I have discovered that the aniline reds, before referred to, may be converted into new coloring matters, still retaining the same color, possessing acid properties, and thus be rendered capable of being employed in the presence of acids or acid mordants. I submit the before-[855]*855mentioned rosaniline, separately or conjointly, to the action of sulphuric add in such a manner as to convert it into a sulpho-conjugated rosaniline, tho same being a new article possessing properties different from any rosaniline ever produced before my invention. In order to make the desired conversion, I use about ten pounds of rosaniline, or its salts, (by preference anhydrous chloride of rosaniline,) and dissolve it in about fifty pounds of fuming sulphuric acid. I operate, either at tlie ordinary or at a moderate temperature, until the conversion into the new coloring matter or compound is complete. The desired result may be ascertained by testing a portion of the mixture, and, when the coloring-matter contained therein is found to be soluble in caustic alkali, the operation may be considered at an end. * * * I have found that in making combinations such as described it is well to employ fuming sulphuric acid, gauging from 69 to 70 degrees Beaume.
“I claim as my invention (1) the sulpho-conjugated compound of rosaniline, possessing the properties specified, as a new article of manufacture; (2) the method herein specified of manufacturing the within-described sulphoconjugated compound of rosaniline, substantially as sot forth.”

Tho material parts of the Caro patent are as follows:

“This invention relates to a dye-stuff or red coloring matter, which is obtained 1)\ acting upon fuehsine with crystalizable sulphuric acid, commonly called ‘ anhydrous sulphuric acid,’ hv which is formed a tri-sulpho compound of rosaniline. The dye-stuff called ‘ fuehsine ’ is also known under the names o? <róseme,’ ‘magenta,’ and ‘ruby.’ In carrying out my invention, I take ten kilograms of fuehsine, which lias been dried at 110 degrees centigrade, and add thereto, little by little, forty kilograms of crystalizable sulphuric acid, commonly called ‘ anhydrous sulphuric acid,’ under constant agitation, while the temperature of the mixture must not be allowed to sink below 120 degrees centigrade, nor to rise above 170 degrees centigrade. A sample of tho mass is supersaturated, from time to time, with an alkali, such as soda, lye, and, if a clear yellowish solution is produced without a precipitate, the conversion is completed. The thick fluid mass which is obtained by this conversion is easily soluble in water, and, after it has been dissolved, it is treated with milk oí lime. * *
“Tho characteristics of the new dye-stuff or coloring matter prepared from fuchsino, in the maimer above described, are as follows: First, by a surplus of alkali, its aqueous solution is changed from a fuehsine red to a light yellow; seoond, flic dyeing on woo] is done in a boiling dye-bath, with tlio addition of mineral acids, or with acid mordants, such as are commonly used in dyeing or printing; third, it produces on wool nearly the same, shades of color which are produced with ordinary fuehsine, from which it is derived; fourth, the color obtained on wool is only changed with'groat difficulty by strong acids; fifth, this product is tho compound whose name, in strict chemical language, is ‘ tri-sulpho acid of rosaniline.’
“What I claim as new, and desire to secure by letters patent, is, (1) as a new article of manufacture, the dye-stuff or red coloring matter having the characteristics above set forth; (2) the within-described process for producing a new' dye-stuff or red coloring matter, by tho action of crystal!izable sulphuric acid, commonly called ‘ anhydrous sulphuric acid,’ on ‘ fuehsine,’ substantially in tho manner set forth.”

The testimony of the experts for the plaintiffs, to tho effect that, although the descriptions of tho process differ in tho respective patents somewhat, those skilled in tho art cannot fall to recognize their essential identity, and that both processes will produce a tri-sulpho acid of rosauiliue, is accepted as established by tho proofs; and the proofs demon[856]*856strate, beyond a fair doubt, that this is so, unless an hypercritical and irrational meaning is applied to the descriptive terms of the process of the Holliday patent, and the process is practiced in accordance with such an interpretation.

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Bluebook (online)
29 F. 853, 24 Blatchf. 201, 1887 U.S. App. LEXIS 2407, Counsel Stack Legal Research, https://law.counselstack.com/opinion/holliday-v-pickhardt-circtsdny-1887.