US2322070A

US2322070A - Method for converting hydrocarbon oils

Info

Publication number: US2322070A
Application number: US340012A
Authority: US
Inventors: Reginald K Stratford; Roy H Smith
Original assignee: Standard Oil Development Co
Current assignee: Standard Oil Development Co
Priority date: 1940-06-12
Filing date: 1940-06-12
Publication date: 1943-06-15
Anticipated expiration: 1960-06-15

Description

NNQOOU Filedv June 12. 1946 rTl la "0k GNIRWM. l.

R K. STRATFORD ETAL METHOD FOR GONVERTING HYDROGARBON OILS IIIII June' 15, 1943.

Patented June l5, 15943 'A n 2,322,010 f METHOD FOR CGNVERTING HYDRO- CABBON GILS Reginald K. Stratford, Corunna, Ontario, and Roy H. Smith, Sarnia, Ontario, Canada, assignors to Standard Gil. Development Company, a cor poration of Delaware Application JunelZ, 1940, Serial No. 340,012

2 Claims.

The present invention relates to the art of converting high boiling to low boiling hydrocarbons, and more particularly to a catalytic process for producing motor fuels of improved quality. The invention will be fully understood from the following description and drawing.

The drawing is a semi-diagrammatic viewY in sectional elevation showing the path of the oil through the equipment. I

The present invention is a continuation-inpart of a prior application Serial No. 248,164, iiled December 29, 1938.

Many cracking methods are known and a wide range of cracking conditions has been disclosed. It has been desirable to improve the quality of gasoline produced and it has been found necessary to carefully adapt cracking methods and conditions to particular feed stock available for` cracking. In the present invention a further improvement is made by clearly specifying narrow ranges of temperature and pressure for certain feed stocks when employed in a particular cracking method with certain catalytic agents in a particular condition. It has been found that greatly improved results are obtained by a combination of all of these various factors which appear to be equally necessary in order to gain the results desired.

Referring to the drawing, numeral i denotes a feed tank from which the oil to be cracked is taken by pump 2. This feed stock is a type known as an overhead or distillate stock, preferably a gas oil, free from large quantities ci asphaltic or tarry constituents and boiling above 400 F. Numeral 4 denotes a second tank from which a lighter oil is taken by a pump 5. This second stock is a heavy naphtha or kerosene distillate. The two stocks from the tanks I and 4 may be admixed prior to passage through a catalyst mixing chamber 3, or either the one or the other may be passed through the said mixer, but the preferred manner is to pass the heavy naphtha from tank I through the mixer 3 where the catalyst is added and this mixture is then passed through a heater coil 6 so as to reach a high temperature and to eifect at least partial reforming of the said stock. The reformed oil vapor then passes through a reducing valve 'i and meets the gas oil stream which has preferably been preheated in the preheater 9.

The mixed oil along with the catalyst is then further heated and cracked in a coil i and is discharged into separator tower i2 through a release valve il. It is preferred to add quenching oil by means of a pipe i3. The separator is fitted with reuxing coil l and fractionating plates i5 in the usual manner and a pan i6, or other equivalent means, is provided for withdrawing an intermediate cut. Heavy tarry oil containing the catalyst is taken from the base of the tower i2 by a pipe i1 which leads to a coil i8 and thence to a lter i9 which is employed for removingcatalyst from the oil. Oil is taken by a pipe 20 to storage, not shown. 'I'he filter may be provided withA a precoat of fresh catalyst in clean oil by a pipe 2i and the catalyst may be lstripped from the iilter and returned to the catalyst mixing chamber 3 preferably after regeneration, but the amount of catalyst is so small and cheap that it may be economically discarded. Intermediate oil from the pan i6 is drawn oi by pipe 22, thru cooler 23, thence by pipe 26 and pump 25 it may be supplied as the quenching oil previously mentioned as being added at pipe i3. A portion may be drawn oil? by line 26 and used as a heating oil. The overhead from tower i2 containing naphtha, lighter easily liqueiiable hydrocarbons and fixed gases, is-passed by a vapor pipe 21 to a condenser 28 and separator 29 from which the fixed gas is taken oi by a; pipe 30. The liquid fraction passesto a stabilizer tower 3| of the usual construction. Stabilized gasoline is removed by a pipe 32 while the lighter, easily liqueflable hydrocarbons, m'ainly containing 3 and 4 carbon atoms, are taken overhead. These fractions may be withdrawn by a pipe 33 or returned by a pipe 35, either alone or together with the fixed gases for repassage through the reformer and cracking coils.

In the operation of the present process it is l important that the ges oil be cracked under the influence of a stream of iinely divided catalyst while completely in the vapor phase and for this purpose a substantial volume of lighter hydrocarbon fractions is added sumcient in quantity e to completely bring the gas oil into the vapor phase. While such gas oils have been cracked in vapor phase previously, it has been done only at low pressures, for example, at atmospheric or at the most about pounds per square inch,

but in the present process pressures of at least 300 pounds per square inch are required and frequently the pressure may amount to 1000 pounds or more. Temperature is likewise higher than is usual say from 1000 to 1100 F. Such temperatures have been used commercially but only at low pressures and it has not been considered feasible at the high pressures 'specified above. It

' heavier oil to be cracked depending on the temperature and the pressure used, that is to say, the naphtha content measured as fractions boiling below about 400 F. should amount to at least of the gas oil to be cracked. Naturally if the gas oil contains an excessive or unusual amount of heavy fractions, the proportion of naphtha is greater than when a gas oil of the usual characteristics is used. With lower temperatures and pressures. the amount of the naphtha may be in the range from 10 to 15% only, but better results are obtained with higher pressures of 500 to 700 pounds per square inch and under these conditions it is necessary to use to 30% of naphtha. The naphtha may be admixed directly with the gas oil if desired, but it is preferred to effect some naphtha reforming in the coil 6 in absence of the gas oil. This coil G is operated at a temperature from 950 to 1l00 F. under pressure and the reaction is preferably conducted in the presence of the catalytic agent. The pressure should be sufilcient so as to not only force the oil through this coil but likewise to maintain a pressure of 300 to 1000 pounds per square inch in coil I0, which is used for the cracking and is fed directly from coil 6 as shown.

Instead of naphtha, butane and propane or either the one or the other may be used as the vaporizing medium but it is generally desirable to return the propane and butane fractions produced in the operation and to add thereto some 15 to 25% of heavy naphtha based on the gas oil treated. In this way a balanced operation is obtained. Even the heaviest distillate gas oils can be brought into vapor phase in the coil and cracked satisfactorily while in the presence of the catalyst and in addition the heavy naphtha is reformed. By complete vaporization is meant the absence of a liquid phase however small.

4Another factor which has been mentioned but not specifically disclosed above is the catalyst to be employed. The preferred catalysts are the natural earths, such as fullers earth, bentonite, and preferably those which have been treated with sulfuric acid, hydrochloric or hydrofiuoric acids, and which are therefore in the class of the activated natural earths. In addition to these, synthetic earths may also be employed, such as the gels of silica, activated alumina or mixtures or co-precipitated gels, hydro gels and the like, especially gels of silica and alumina or silica and magnesia. These gels may be used alone or they may be modified by the addition of metal agents containing, for example, nickel, iron, cobalt, manganese, vanadium, chromium, molybdenum, tungsten, their oxides, sulphides y and the like.

The amount of the catalyst is quite small; for

example. good results are obtained with 116 to 10 pounds of the catalyst per barrel of the oil to be cracked. The catalyst, a nely divided powder or in granular form, together with the oil passes easily through the heating coils and other equipment without settling out or causing any dimculty. It may be removed by filtering or tures either cannot be reached at all or if reached, l

the operation must be discontinued after a short time because of coking dificulties. Even if the catalyst be present and the'operation is not conducted completely in the vapor phase. coking diiculties will also make themselves felt within a relatively short time. If small amounts of the catalytic agent are present and suflicient of the light hydrocarbon is also present to maintain the heavy oil completely in a vapor phase. excellent results can be obtained for long periods of time without coking diiculties, giving rise to an excellent grade of naphtha.

It is somewhat difficult to specify denitely the specific temperatures, pressures and the amount of the lower boiling oil to be present at the same time. The above mentioned ranges are given approximately, but it will be understood that these several conditions must be mutually adjusted within the ranges given so as to bring about the reaction completely in the vapor phase. Experience has shown that this is the prerequisite for excellent results.

With the above combination of cracking conditions, feed mixtures and catalysts, it is possible to obtain high grade naphthas with octane num bers from rI2 to 75 without any coking difficulties and without dangerously over-heating the cracking coils.

As an example of the present operation, a feed stock consisting of 65% of heavy gas oil, 25% of lighter gas oil and 10% of heavy naphtha was admixed with 1.4 pounds of clay per barrel of the gas oil and this mixture was passed once through a heated coil wherein temperature was raised rapidly to l060 F. while under a pressure of .350 pounds per square inch. I'he run was continued for several days Without any difliculty in operation and the products were separated in the usual manner. The naphtha distillate produced amounted to 52 vol. per cent of the oil charged; A gas oil suitable as a domestic heating oil amounted to 13 vol. per cent, the gas was 12 wt. per cent and 4.5 vol. per cent excess butane and a tarry fuel oil of 20 vol. per cent was produced. No coke was produced and after removal of the clay catalyst from the tarry oil, it was found suitable for fuel oil. 'I'he naphtha had an' octane number of 73.3.

In other runs it has been found that the temperature could not be reached without the catalyst because of overheated tubes and coking difficulties. Likewise coke dimculties rapidly developed if the naphtha was omitted from the feed. With lower pressures the yields of gasoline dropped off rapidly.

` The present invention is not to be limited by any theory of the reaction or any particular types of feed oils or conditions except as specified in the claims.

We claim:

1. An improved cracking process which comprisespassing heavy naphtha through a heating coil under pressure above 400 pounds per square inch and at a tempeture sumcient to reform the naphtha, tiren admixing the reformed naphtha while hotfjwith a heavier distillate oil to be cracked, and passing this mixture through a second heating coil under pressure of at least 300 pounds per square inch and temperatures between 1000 and 1100 F., while in a completely vaporized condition and in the presence of a tinely divided siliceous cracking catalyst whereby a substantial portion of the heavier distillate is cracked to gasoline, then separating the 'gasoline so produced.

2. An improved cracking. process which comprises mixing a finely divided siliceous cracking catalyst with a heavy naphtha fraction, passing the resulting mixture through a heating coil under a pressure of about 400 pounds per square inch and at a temperature suiilcient to lreform the naphtha,`then admixing the reformed naphtha while hot with a heavier distillate oil to be cracked, passing the last-named mixture through a second heating \coil under a pressure of at least 300 pounds per square inch and at a temperature between 1000* F. and 1100 F. while in a completely vaporized condition whereby a substantial portion of said heavier distillate is cracked into gasoline in the presence of said finely divided siliceous cracking catalyst and heavy naphtha fraction, and thereafter separating the gasoline from the cracked products.

REGINALD K. STRATFORD. ROY H. SMITH.