Application of John B. Dwyer, Joseph W. Jewell, William B. Johnson, Henry G. McGrath and Louis C. Rubin

317 F.2d 203, 50 C.C.P.A. 1230, 137 U.S.P.Q. (BNA) 540, 1963 CCPA LEXIS 348
CourtCourt of Customs and Patent Appeals
DecidedMay 16, 1963
DocketPatent Appeal 6957
StatusPublished
Cited by5 cases

This text of 317 F.2d 203 (Application of John B. Dwyer, Joseph W. Jewell, William B. Johnson, Henry G. McGrath and Louis C. Rubin) 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 John B. Dwyer, Joseph W. Jewell, William B. Johnson, Henry G. McGrath and Louis C. Rubin, 317 F.2d 203, 50 C.C.P.A. 1230, 137 U.S.P.Q. (BNA) 540, 1963 CCPA LEXIS 348 (ccpa 1963).

Opinion

WORLEY, Chief Judge.

This is an appeal from the decision of the Board of Appeals affirming the examiner’s rejection of claims 1 through 8 in appellants’ application 1 entitled “Reforming of Gaseous Hydrocarbons” as unpatentable over the prior art.

The application discloses a process for converting normally gaseous hydrocarbons such as methane or natural gas with steam and/or carbon dioxide to produce hydrogen and carbon monoxide. Appellants concede that process, referred to as hydrocarbon reforming, to be old. They say, however, that it has been the desire of the art to achieve reforming at higher pressures and higher space velocities 2 while maintaining an acceptable percentage of conversion, alleging that such procedure results in the following advantages :

“ * * * Higher space velocities are desirable because it means a higher conversion to hydrogen and carbon monoxide per pound of metal tubing in the furnace thus decreasing the very high cost of the furnace. It is further desirable to increase both the pressure and space velocity in order to increase the capacity of the furnace and thus reduce required catalyst inventory. Pressure operations are particularly advantageous as the higher space velocities and much greater endothermic heat of reaction per tube results in greater heat transfer per unit tube surface area without any increase in metal temperature. Pressure operations also decrease the cost of subsequent compression, such as when using the hydrogen and carbon monoxide gas formed for the production of hydrocarbons by the Fischer-Tropsch reaction under elevated pressures, or in ammonia synthesis, or synthesis of methanol or isobutanol.”

Representative claims are 1 and 8:

“1. A process for reforming a low boiling hydrocarbon to produce a product containing hydrogen which comprises passing a preheated low boiling hydrocarbon and steam at a steam to methane equivalent ratio of at least 1.8:1 through a multitubular reaction zone in the presence of a nickel oxide catalyst at space velocities at standard conditions corresponding to at least 700 volumes of methane equivalent per hour per volume of catalyst at an outlet pressure of at least 50 pounds per square inch gage, maintaining the outlet temperature of said tubular reaction zone between about 1350°F. and about 1700°F. by indirect heat exchange with a burning fuel and producing an effluent gas containing hydrogen without an excessive amount of unconverted low boiling hydrocarbon.
“8. In a process for reforming methane to produce hydrogen and carbon monoxide in which steam and methane are preheated to a temperature between about 800°F. and *205 about 1150°F. and are passed through a multitubular reaction zone in the presence of a nickel oxide supported catalyst and the outlet temperature of said reaction zone is maintained between about 1350°F. and about 1700°F. by indirect heat exchange with a burning fuel, the improvement which comprises maintaining the outlet pressure of said reaction zone at least 50 pounds per square inch gage, maintaining a steam to methane mol ratio between about 2.1:1 and about 2.6:1 and providing a residence time for the reactants corresponding to a space velocity of at least 700 volumes of methane equivalent per hour per volume of catalyst whereby an effluent gas containing hydrogen and carbon monoxide and not more than 6 mol per cent unconverted methane is produced.”

The references relied on are:

Mayland 2,622,089 December 16, 1952. Roberts, Jr. 2,625,470 January 13, 1953.

Mayland discloses a process for the manufacture of carbon monoxide and hydrogen from hydrocarbons, carbon dioxide and steam. Hydrocarbons such as natural gas, methane, ethane, propane and butane are said to be useful. He states that in conventional reforming units natural gas is passed over a reduced nickel oxide catalyst at about 1400°F. in the presence of carbon dioxide and steam, but says his invention resides “in the fact that an improved method of operation of a gas reforming unit for natural gas in the presence of steam and carbon dioxide can be effected by employing high space velocities,” and that “[hjigher yields of reformed gases of high quality are obtained for any given equipment size.”

Roberts also teaches the preparation of hydrogen and carbon monoxide from gaseous hydrocarbons by reacting them with carbon dioxide and water, i. e., by the catalytic reforming of methane or natural gas in a tubular reformer. He states that while the chemistry of reforming is simple and straightforward, engineering problems arise because practicable reforming reactions require very high temperatures and large quantities of heat input. He says that one way of getting additional heat to the products undergoing reaction is by preheating the feed gas, stating that it is desirable to carry out the reforming operation at maximum pressures since the feed gases are often available under substantial pressure, and also since the product gases are frequently used under pressure. The rest of Roberts is cumulative to Mayland.

The board, in affirming the examiner, stated:

“After a careful and complete consideration of all the arguments advanced by the Examiner and on behalf of appellants, we are of the view that the Examiner’s rejections are without reversible error and for the reasons stated by the Examiner, the rejections will be sustained.” (Italics supplied).

The examiner held that Mayland discloses a supported nickel oxide catalyst, temperatures from 1100° to 2000°F., and pressures from atmospheric to 250 p. s. i. The examiner made particular reference to the fact that Mayland discloses methane, ethane, propane, along with other gases, as suitable hydrocarbons, and that a “space velocity of 400 for ethane or propane would be equal to space velocities of 800 or 1200, respectively, when expressed in terms of methane equivalents.” 3 The examiner *206 concluded his evaluation of the Mayland reference with the statement:

“ * * * At best, applicants are merely operating their process within the patentee’s disclosed reaction conditions and such a method of operation would not involve invention. Applicants’ recited pressures are not considered to be critical to their process, note page 3 of the specification which discloses the process may be operated at about 25 p. s. i.”

The examiner rejected the claims as “substantially met by” Mayland. That terminology as employed by the Patent Office is equivalent to “unpatentable over.” 4 Consequently, we take it that the rejection is based on “obviousness” within the meaning of 35 U.S.C. § 103. Since the process itself is admittedly old, the issue is whether the reaction conditions recited in the claims, and upon which patentability is predicated, would be obvious to one of ordinary skill in view of the teachings of the prior art. More specifically, the question is whether the combination of pressure above 50 p. s. i.

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317 F.2d 203, 50 C.C.P.A. 1230, 137 U.S.P.Q. (BNA) 540, 1963 CCPA LEXIS 348, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-john-b-dwyer-joseph-w-jewell-william-b-johnson-henry-ccpa-1963.