In re Harrison

77 F.2d 635, 22 C.C.P.A. 1341, 1935 CCPA LEXIS 202
CourtCourt of Customs and Patent Appeals
DecidedJune 10, 1935
DocketNo. 3491
StatusPublished
Cited by1 cases

This text of 77 F.2d 635 (In re Harrison) 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 Harrison, 77 F.2d 635, 22 C.C.P.A. 1341, 1935 CCPA LEXIS 202 (ccpa 1935).

Opinion

Hatfield, Judge,

delivered the opinion of the court:

This is an appeal from the decision of the Board of Appeals of the United States Patent Office affirming the decision of the Primary Examiner rejecting claims 16,17,18, 20, 21, 23, and 31 in appellant’s application for a patent for an alleged invention relating to a process for converting hydrocarbon oils into lighter hydrocarbons.

Claims 16, 18, and 20 are sufficiently illustrative. They read:

16. In a process of heat-treating hydrocarbons, heating a petroleum stream to liquid-phase cracking temperatures, simultaneously heating another petroleum stream to vapor-phase cracking temperatures at less pressure, and discharging both highly heated substantially uncooled streams directly into mixture together in a further zone while abruptly lowering the pressure of the stream from the liquid-phase operation, the zone of admixture being under a super-atmospheric pressure.
18. In a process of heat-treating hydrocarbons, heating a petroleum stream to liquid-phase cracking temperatures, simultaneously heating another petroleum stream to vapor-phase cracking temperatures at less pressure, passing the vapor phase stream to a time reaction zone guarded against substantial heat loss, and discharging the highly heated vapor-phase cracking stream and the liquid-phase cracking stream into admixture together in a further zone while abruptly lowering the pressure of the stream from the liquid-phase operation, the zone of admixture being under a super-atmospheric pressure.
20. In a process of heat-treating hydrocarbons, heating a petroleum stream to liquid-phase cracking temperatures, simultaneously heating another petroleum stream to vapor-phase cracking temperatures at less pressure, discharging both such highly heated substantially uncooled streams into admixture together in a further zone while abruptly lowering the pressure of the liquid-phase stream, the zone of admixture being under a super-atmospheric pressure,, taking off and fractionating the vaporous products from the zone of admixture, and returning a naphtha fraction as the petroleum supply stream to the vapor-phase cracking operation.

The references are :

Lang, 954,575, Apr. 12, 1910.
Perelis, 1,701,477, Feb. 5, 1929'.
Isom, .1,708,180, Apr. 9, 19291.
Isom, 1,722,223., July 23, 1929’.
Greenstreet, 1,740,691, Dec. 24, 1929'.
Herthel, et al., 1,747,437, Feb. 18, 1980.
Pratt, 1,752,264, Mar. 26, 1930.
Tinker, 1,779',2.22, Oct. 21, 1930.
Fixman, 1,781,872, Nov. 18, 1930'.

We think the appealed claims sufficiently describe appellant’s process.

Claims 19 and 22 were allowed by the Primary Examiner. Claim 19 is illustrative. It reads:

[1343]*134319. In a process of beat-treating hydrocarbons, beating a petroleum stream, to a liquid-phase cracking temperature not exceeding 975° F. and a pressure of 400-1200 pounds per square inch, simultaneously heating' another petroleum stream to a vapor-phase cracking temperature of 10555-1125° F. and a pressure not exceding 200 pounds per square inch, passing the vapor-phase stream to a time reaction zone guarded against substantial heat loss wherein the velocity is diminished, and discharging the highly heated vapor-phase cracking stream and the entire liquid-phase cracking stream into admixture together in a further zone while abruptly lowering the pressure of the stream from the liquid-phase operation to not exceeding 200 pounds per square inch.

It will be observed tliat claim 19 contains the limitation “ passing (he vapor-phase stream to a time reaction zone guarded against substantial heat loss wherein the velocity is diminished!''' (Italics ours.)

The Primary Examiner described the references as follows:

Lang shows an early use of a double tube system for cracking first a heavy hydrocarbon in tubes 5 and tubes 8 and vaporizing in these latter tubes and fractionating and returning light fractions to be heated to cracking temperatures coil 29 and vaporizing zones 8. Lang mentions no. temperatures relying on the skill of the operator but he does destructively heat the vapors, see page 2, line 125.
Isom heats heavy oil to high pressure in coil 5 and temperatures of 750'° to 800° F., the pressure dropping in drum 55, to. atmospheric or higher pressures may be used, and maintains temperatures of 1000° to 1200'° F. on coil 23 and only enough pressure to force the oil in the drum. Isom maintains a small time reaction zone 26 which also serves to. remove residual heavy polymers and carbon. The light fractions from fractionators 12 and 16 are returned as charging stock.
Isom 1,722,223 is similar to the above Isom patent. Isom uses naphtha bottoms as charging stock for the high temperature coll.
Greenstreet has similar conditions but no time reaction zone, unless the last sections of the coil be considered as time reaction zones which is so done in Perelis of record. A tube is a time reaction zone unless differentiated bv «-not* a phrase as — diminishing the velocity of the heated hydrocarbons — .
Herthel maintains optimum conditions in each coil 4 and 6 to crack, the respective charging stocks admitted, one lighter than the other.
Pratt cracks oil in 17 at pressures apparently under 200 lbs. per ,sq. inch, at 800° F. thereabouts, then vaporizes in D at a pressure less than maintainea in the distillate high temperature coil 32 (around atmospheric plus pressure necessary to force it thru the coil which is considerable at the pump end. The coil 32 can be considered to have a time reaction section in the low temperature portion of the furnace and the oil is heated to 1100° F. under low pressure.
Tinker and Fixman show reduced pressure zones on their light distillate cracking coils which also serve as time reaction zones. Note valve 68 of Fix-man and valve V', Fig. 5 of Tinker * * *,

and held that the appealed claims were substantially met by the patents to Isom and Pratt. He further stated:

Applicant has attempted to distinguish over Pratt by the phrase “ discharging both highly heated substantially uncooled streams directly into admixture together ” to show a difference between the time reaction step of Pratt in coil [1344]*134436 but this step is already old in the other references and the time reaction zones of Pratt and the applicant are considered to be substantially the same in effect insofar as' they are claimed.

In its decision, tbe Board of Appeals stated that the examiner had relied mainly on-the Isom and Pratt patents, and, after describing the Isom patents, stated that:

In neither one of the'se patents is there any abrupt lowering of the pressure of the liquid phase stream as it enters the drum 55 as called for by the claims. As shown, the pressure in the coil 5 is the same as in the drum 55. It is.

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77 F.2d 635, 22 C.C.P.A. 1341, 1935 CCPA LEXIS 202, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-harrison-ccpa-1935.