Application of Edward J. Hoffman

406 F.2d 1398, 56 C.C.P.A. 964
CourtCourt of Customs and Patent Appeals
DecidedMarch 6, 1969
DocketPatent Appeal 8072
StatusPublished

This text of 406 F.2d 1398 (Application of Edward J. Hoffman) 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 Edward J. Hoffman, 406 F.2d 1398, 56 C.C.P.A. 964 (ccpa 1969).

Opinion

RICH, Judge.

This appeal is from the decision of the Patent Office Board of Appeals, adhered to on reconsideration, affirming the rejection of claims 4 through 9 of application serial No. 198,318, filed May 28, 1962, entitled “Process for Resolution of Hydrocarbon Streams.” No claim has been allowed.

The invention relates to a process for separating a multicomponent hydrocarbon mixture, e.g., a natural gas feed, into high- and low-boiling fractions. Claims 5 through 9 are all ultimately dependent on claim 8. At oral argument, appellant’s attorney stated that “all claims stand or fall together”; we therefore need consider only the rejection of claim 8, which reads (our emphasis):

8. A continuous process for the sharp resolution of a multicomponent mixture of hydrocarbons of wide volatility range comprising:
(a) introducing a feed stream comprising a multicomponent mixture of hydrocarbons of wide volatility range intermediate the top and bottom of a column to contact said stream with a downflowing stream of an absorption solvent of low volatility to provide an absorption section in the portion of said column above said feed point to absorb substantially all the hydrocarbons [sic] constituents having boiling points not lower than a desired separation point, and, to a lesser extent, to absorb a portion of the hydrocarbons having boiling points not higher than said desired separation point;
(b) collecting an overhead product from said column consisting essentially of hydrocarbon constituents having boiling points not higher than that of the desired separation point;
(c) removing an enriched solvent stream containing said hydrocarbon *1400 constituents as a bottoms stream from said column;
(d) passing said column bottoms stream as feed to a distillation process;
(e) distilling said column bottoms stream to vaporize an overhead stream consisting essentially of hydrocarbon constituents having a boiling point not higher that [sic]’ that of said absorption solvent and to form a bottoms stream of solvent and hydrocarbon constituents having a boiling point not lower than that of said solvent;
(f) partially condensing said vaporized overhead stream to form a gaseous phase and a liquid product phase consisting essentially of hydrocarbon constituents having boiling points not lower than said desired separation point;
(g) passing at least a portion of said gaseous phase to said column at a point below the feed point of said hydrocarbon stream to contact said downflowing solvent with said gaseous phase to provide a stripping section in said column below said feed point.

The overall process can best be understood by reading claim 8 in conjunction with the following diagram of the claimed process: 1

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The only issue is whether the claimed invention is obvious in view of the prior art and therefore unpatentable under 35 U.S.C. § 103. The rejection is based on two United States patents:

Parsons et al. 3,060,662 Oct. 30, 1962

Kassel 2,685,941 Aug. 10, 1954

*1401 Figure II, 2 infra, is a simplification of Figure 1 of the Parsons et al. patent (hereinafter "Parsons”) showing the key features of the Parsons process.

With reference to Figure II, a natural gas feed stream 11 is ultimately separated into a propane-and-higher-boiling fraction and an ethane-and-lower-boiling fraction. The feed is introduced to absorber 12 where it is contacted with down-flowing absorption oil which preferentially absorbs propane and higher-boiling hydrocarbons. Ethane and lower-boiling hydrocarbons, containing some propane and heavier hydrocarbons, are collected as the overhead product of absorber 12. Rich oil 15 removed from the bottom of the. absorber contains most of the propane and heavier hydrocarbons and a good deal of ethane and lighter hydrocarbons from the feed stream. Some of the absorbed hydrocarbons are removed from the oil by the flashing step 27 and are recycled to the reabsorber via line 28. Rich oil leaving the flasher is subjected to distillation wherein the remaining absorbed hydrocarbons are separated from the oil. Lean oil 43, obtained as distillation bottoms, is recycled to the absorber and re-absorber. Stream 18 separated by the distillation is subjected to condensation (not shown) and flashing to produce a liquid phase 21 and a gaseous phase 20. *1402 The gaseous phase is recycled to, the re-absorber, and the liquid phase is separated by distillation into an overhead 53 of ethane and lighter materials and an ultimate propane fraction. The overhead is recycled to the reabsorber. Parsons also shows “another gasoline plant” 12a which provides a stream introduced into the reabsorber via recycle stream 20.

Kassel relates to a method of producing purified hydrogen from gaseous mixtures containing C1-C5 hydrocarbons. Referring to the “Secondary Absorber” in Figure III, a multicomponent gaseous feed stream Gi containing hydrogen, methane, ethane, and propane is introduced intermediate the ends of the secondary absorber 14. The gas rising in the secondary absorber is contacted with a secondary absorber oil stream L3 which comes from the secondary stripper and enters the top of the absorber. A product stream G2 rich in hydrogen is removed as overheads, and rich secondary absorber oil stream L4 is removed as bottoms. Stream L4 is subjected to flashing in chambers 21, 27, and 32 and then to stripping in the secondary stripper 24. Overheads from the secondary stripper are recycled via G5 to the secondary absorber where they are introduced below the point of introduction of feed stream Gi.

It was the examiner’s position that considering reabsorber 23 of Parsons to be the absorber recited in claim 8, stream 28 to be the feed stream, and combined streams 20 and 53 to be recycle streams, the sole significant difference between the claimed process and that of Parsons is that in the former the recycle stream is introduced to the absorber at a point below that at which the feed is introduced (see claim step “g”), whereas in the latter the feed and recycle streams are introduced at the same point, near the bottom of the absorber. This is also *1403 the only difference urged by appellant in support of his contention that his process is not obvious. With respect to this difference, the examiner noted that in Kassel recycle stream G5 is introduced into absorber 14 below feed stream Gi and concluded that:

It would therefore be obvious for one of ordinary skill in the art in view of Kassel to apply the teaching to pass a vapor reflux stream to an absorber below the feed introduced therein in Parsons et al. if not obvious over Parsons et al. per se.

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406 F.2d 1398, 56 C.C.P.A. 964, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-edward-j-hoffman-ccpa-1969.