PROCESS FOR PEAKING THE OXIDATION PRODUCTS OF 1-OLEFINS
United States Patent 3696134
A peaking process is disclosed for preparing aldehydes or carboxylic acids from a mixture of alpha olefins. The alpha olefins are separated into at least two fractions consisting of a low molecular weight fraction and a high molecular weight fraction. The high molecular weight fraction is isomerized and the two fractions oxidized. The low molecular weight fraction will oxidize to Cn-1 product and C1 product. The high molecular weight fraction will cleave at the double bond giving products containing the number of carbon atoms of the groups on either side of the double bond. The procedure has great versatility by varying the number of fractions and isomerizations. With alpha olefins prepared from metal alkyl growth product, M-values also have an influence on the final product.
US Patent References:
Preparation of high purity primary organo aluminum compounds
Johnston - February 1968 - 3369037
Method and apparatus for controlling feed to a polymerization reaction
Smith et al. - May 1966 - 3250757
/3557169.html
Robinson - January 1971 - 3557169
Preparation of high purity primary organo aluminum compounds
Johnston - February 1968 - 3369037
Method and apparatus for controlling feed to a polymerization reaction
Smith et al. - May 1966 - 3250757
/3557169.html
Robinson - January 1971 - 3557169
Application Number:
05/001655
Publication Date:
10/03/1972
Filing Date:
01/09/1970
View Patent Images:
Export Citation:
Primary Class:
Other Classes:
568/469, 568/475, 562/544
International Classes:
C07C45/28; C07C45/34; C07C53/126; C07C45/00; C07C53/00; C08H17/36
Field of Search:
260/413,533R,64R
Other References:
Pattison, Fatty Acids and Their Industrial Applications Marcel Dekker, Inc., New York, 1968 pp. 363-364..
Primary Examiner:
Gotts, Lewis
Assistant Examiner:
Love, Ethel G.
Claims:
Having thus described the invention, I claim
1. A peaking process for preparing oxidized products selected from the group consisting of aldehydes and acids from a mixture of alpha olefins, said process comprising separating said alpha olefins into at least two fractions wherein one fraction contains the relatively lower molecular weight olefins from said alpha olefin mixture, and the other the relatively higher molecular weight olefins from said alpha olefin mixture, isomerizing the fraction containing the higher molecular weight olefins to internal olefins, and then oxidizing the two fractions simultaneously in the same action zone.
2. The process of claim 1 wherein the alpha olefins are obtained by displacement of aluminum trialkyls.
3. The process of claim 2 wherein the alpha olefins contain even carbon atom olefins of two to 30 carbon atoms.
4. The process of claim 3 wherein the olefins are fractionated into at least three fractions and the lowest molecular weight fraction is recycled to the aluminum trialkyl zone for regrowing, a low molecular weight fraction but higher than the lowest molecular weight fraction is oxidized and a higher molecular weigh fraction is isomerized and oxidized.
5. The process of claim 4 wherein the lowest molecular weight fraction consists of ethylene and butene-1.
6. The process of claim 5 wherein the low molecular weight fraction to be oxidized consists of C6 to C12 alpha olefins and the higher molecular eight fraction consists of C14 to C30 alpha olefins.
1. A peaking process for preparing oxidized products selected from the group consisting of aldehydes and acids from a mixture of alpha olefins, said process comprising separating said alpha olefins into at least two fractions wherein one fraction contains the relatively lower molecular weight olefins from said alpha olefin mixture, and the other the relatively higher molecular weight olefins from said alpha olefin mixture, isomerizing the fraction containing the higher molecular weight olefins to internal olefins, and then oxidizing the two fractions simultaneously in the same action zone.
2. The process of claim 1 wherein the alpha olefins are obtained by displacement of aluminum trialkyls.
3. The process of claim 2 wherein the alpha olefins contain even carbon atom olefins of two to 30 carbon atoms.
4. The process of claim 3 wherein the olefins are fractionated into at least three fractions and the lowest molecular weight fraction is recycled to the aluminum trialkyl zone for regrowing, a low molecular weight fraction but higher than the lowest molecular weight fraction is oxidized and a higher molecular weigh fraction is isomerized and oxidized.
5. The process of claim 4 wherein the lowest molecular weight fraction consists of ethylene and butene-1.
6. The process of claim 5 wherein the low molecular weight fraction to be oxidized consists of C6 to C12 alpha olefins and the higher molecular eight fraction consists of C14 to C30 alpha olefins.
Description:
BACKGROUND OF THE INVENTION
This invention relates to oxidation of a mixture of alpha olefins so as to obtain oxidation products, such as aldehydes and carboxylic acids, having carbon atoms in a narrower range than did the original mixture.
It is known to produce alpha olefins in the prior art. It is known, for example, that alpha olefins can be prepared from organometal compounds such as aluminum trialkyls by olefin displacement, thermal displacement, or catalytic displacement. See for example U.S. Pat. Nos. 2,971,969, 3,344,202, and 3,280,023. It is also known that long-chain alpha olefins can be prepared by reacting ethylene in presence of catalytic amounts of metal alkyls; see British Pat. Nos. 1,020,563 and 1,037,866 and US Patents Nos. 2,699,457 and 3,322,844. It is also known to produce such alpha olefins by cracking paraffins. The prior art also teaches isomerizing alpha olefins to internal olefins; see U.S. Pat. Nos. 2,956,094, 3,217,061, 3,277,191, and 3,340,322.
It is also known that olefins can be oxidized to aldehydes and/or acids by several means such as ozonolysis, permanganate, chromic acid, osmium tetroxide, and the like.
It is also known in the prior art, see cited patents as examples, that the normal source of olefin production results in a statistical distribution of olefin chain lengths known as a Poisson distribution.
It is also known from the art cited that alpha olefins prepared from metal alkyls, particularly aluminum trialkyls, can be polymerized to various degrees; e.g., M-values, by controlling growth conditions such as temperature, pressure, and time. M-value means the average number of ethylenes added per alkyl substituent.
OBJECTS OF THIS INVENTION
It is an object of this invention to produce oxidized products from alpha olefins having carbon atoms varying over a wide range wherein the product will have carbon atoms varying over a substantially narrower range.
SUMMARY OF THE INVENTION
According to this invention, a mixture of alpha olefins is separated into at least two fractions, one fraction containing olefins having carbon atoms below a predetermined number and one fraction having carbon atoms of said predetermined number and more. At least one high molecular weight fraction, e.g., containing carbon atoms of the predetermined number and more, is isomerized to produce internal olefins preferably predominating in unsaturation near the center of the chain. The nonisomerized lower molecular weight fraction and the isomerized fraction are oxidized to the aldehyde and/or acid thereby producing product having carbon atoms predominately of intermediate chain length.
In this specification and claims, the terms high molecular weight and low molecular weight are relative only and mean that each fraction will consist of compounds containing at least a mixture of two materials of different number of carbon atoms.
BRIEF DESCRIPTION OF THE DRAWING
The drawing is a schematic flow diagram showing a preferred flow scheme for carrying out the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention can best be described by referring to the drawing. An alpha olefin supply 1 is passed to olefin separation zone 2 via conduit 5 wherein the olefins are separated into at least one low molecular weight fraction and at least one high molecular weight fraction. The total number of fractions and choice of separation points will be dependent upon the composition of the original mixture and the desired product. The separation can be any desired process; however, distillation will be generally used. The higher molecular weight fraction is passed via conduit 7 to isomerization zone 3 wherein the alpha olefins are isomerized to internal olefins by process already known. Any olefin fractions not desired to be oxidized are passed via conduit 6 to olefin storage or further processing, such as recycle to the growth reactor, as desired. It should be understood that conduit 6 can represent a plurality of conduits depending upon the number of cuts. The low molecular weight olefins from separation zone 2 pass via conduit 8 to preferably alpha olefin metathesis zone 11 wherein the alpha olefins are converted to internal olefins and ethylene according to the following formula: 2RCH = CH 2 ➝ RCH = CHR + CH 2 = CH 2 . The internal olefin is then separated from the ethylene and passed to oxidation zone 4 via conduit 12 while ethylene passes via conduit 13 to recycle or storage. The metathesis step is not a necessary step to the invention but has the advantage of avoiding the formation of formic acid. The isomerized olefins from zone 3 pass via conduit 9 to the oxidation zone 4. The olefins are oxidized by processes known forming aldehydes or acids depending upon known reaction conditions. The alpha olefins if zone 11 is omitted form C n -1 carboxylic acids or aldehydes and formic acid or formaldehyde. The internal olefins form a mixture of products breaking at the double bond.
As a specific example, a mixture of C 2 to C 30 alpha olefins obtained by displacement of aluminum alkyls is separated in separation zone 2 by distillation into a C 2 --C 4 fraction, a C 6 --C 12 fraction, and a C 14 to C 30 fraction. The C 2 --C 4 fraction is taken overhead via conduit 6 and is returned to the aluminum alkyl preparation for alkylation and further growth. The C 14 --C 30 fraction is passed to isomerization zone 3 via conduit 7 wherein it is isomerized. The effluent from zone 3 is passed along with the C 6 -12 fraction to the oxidation zone 4. A typical product distribution of such olefins having M-values of 4.00, 5.00, and 6.00 is given in Tables I, II, and III respectively. These results are summarized and shown in Table IV. For calculating olefin distribution for different M-values, see U.S. Pat. No. 3,344,202.
The process obviously can be varied to suit many particular needs. Some such modifications are described below. In all cases, it is assumed that there is a supply of C 2 --C 30 alpha olefins derived by ethylene growth of aluminum trialkyl having a typical statistical distribution.
Case 1: Assume a market for C 7 -15 carboxylic acids. The alpha olefins will be separated into three fractions; e.g., C 2 -6, C 8 -16, and C 18 -30. The C 2 -6 fraction is recycled and regrown, the C 18 -30 fraction is isomerized, and the C 8 -16 fraction and the isomerized fraction are oxidized resulting in an increase in the C 7 -15 desired carboxylic acids.
Case 2: Assume that the C 16 --C 18 olefins have greater value for some other purpose, e.g., olefin sulfonates, whereas the C 5 -13 acids and C 19 -21 acids have a market. The total olefins then will be separated into five fractions; e.g., C 2 -4 which is recycled and grown, C 6 -14 fraction is oxidized, C 16 -18 separated for sales, C 20 -22 fraction separately oxidized, and the C 24 -30 fraction isomerized and oxidized with the C 6 -14 fraction.
Case 3: Assume normal production of C 5 --C 15 acids; but, due to poor market conditions, the C 9 -11 acids are not moving. In this case, the olefins would be separated into five fractions with the C 2 -4 fraction being recycled to growth, the C 6 -8 fraction oxidized to acids, the C 10 -12 fraction would be recycled for growth or isomerized and oxidized with the C 6 -8 fraction depending upon demand, the C 18 -16 fraction oxidized, and the C 18 -30 fraction isomerized and oxidized with the C 14 -16 fraction.
It can be seen from the above modifications that by utilizing the variables, M-value, recycle and regrowth, and isomerization, the present invention offers a great deal of versatility in preparing oxidized products from a mixture of alpha olefins.
To show the effect of M-value and recycle on distribution, Tables I through V are presented to show carbon atom distribution on C 6 -30 alpha olefins at various M-values and recycle of C 2 -4 olefins. Table VI summarizes this data. Tables VII through XI show similar effect when C 2 -6 is recycled, whereas Table XII summarizes these tables. Table XIII shows a typical case where there is no recycle or isomerization at various M-values.
TABLE I
PEAKING PROCESS
M = 2.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and 1 35.29 21.53 25.01 26.40 26.86 27.00 2 1.88 0.56 0.15 0.04 0.01 3 13.57 2.30 0.69 0.18 0.04 0.01 4 2.72 0.82 0.22 0.05 0.01 5 18.71 30.73 27.94 27.04 26.78 26.71 6 3.57 1.07 0.29 0.07 0.01 7 15.84 27.33 24.04 22.98 22.68 22.61 8 4.42 1.32 0.35 0.08 0.02 9 9.63 2.19 15.29 14.12 13.79 13.71 10 1.61 1.58 0.42 0.10 0.02 11 4.53 0.74 0.73 6.91 6.55 6.46 12 0.50 0.49 0.49 0.12 0.02 13 1.74 0.22 0.21 0.21 2.59 2.49 14 0.14 0.13 0.13 0.13 0.03 15 0.49 0.06 0.06 0.06 0.05 0.83 16 0.03 0.03 0.03 0.03 0.03 17 0.18 0.01 0.01 0.01 0.01 0.01
TABLE II
PEAKING PROCESS
M = 3.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above 1 27.42 14.98 19.59 22.29 23.64 24.21 2 2.99 1.29 0.50 0.17 0.05 3 6.26 3.67 1.58 0.61 0.21 0.07 4 4.34 1.87 0.72 0.25 0.08 5 12.98 20.71 17.43 15.87 15.22 14.98 6 5.70 2.46 0.95 0.33 0.10 7 16.55 26.28 22.12 20.15 19.32 19.02 8 7.05 3.04 1.18 0.41 0.13 9 15.08 4.33 20.94 18.64 17.68 17.32 10 3.72 3.62 1.40 0.49 0.15 11 10.68 2.11 2.05 13.74 12.67 12.28 12 1.70 1.65 1.63 0.57 0.18 13 6.08 0.90 0.87 0.86 7.58 7.15 14 0.68 0.66 0.65 0.64 0.20 15 3.03 0.34 0.33 0.32 0.32 3.58 16 0.24 0.23 0.23 0.23 0.23 17 1.23 0.11 0.11 0.11 0.11 0.11 18 0.08 0.07 0.07 0.07 0.07 19 0.51 0.03 0.03 0.03 0.03 0.03 20 0.02 0.02 0.02 0.02 0.02 21 0.19 0.01 0.01 0.01 0.01 0.01
TABLE III
PEAKING PROCESS
M = 4.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 22.94 9.50 13.97 17.44 19.72 21.01 2 3.60 1.99 0.99 0.45 0.18 3 2.65 4.42 2.44 1.21 0.55 0.23 4 5.23 2.89 1.44 0.65 0.27 5 7.36 14.31 11.39 9.57 8.57 8.08 6 6.86 3.79 1.89 0.85 0.35 7 12.44 21.65 17.87 15.49 14.18 13.54 8 8.48 4.69 2.33 1.05 0.43 9 15.12 6.12 21.66 18.77 17.19 16.41 10 5.73 5.59 2.78 1.25 0.52 11 14.24 3.80 3.71 18.25 16.42 15.53 12 3.37 3.29 3.23 1.46 0.60 13 10.92 2.08 2.03 1.99 13.10 12.11 14 1.75 1.71 1.68 1.66 0.68 15 7.13 1.02 0.99 0.97 0.96 8.13 16 0.81 0.79 0.78 0.77 0.76 17 3.98 0.45 0.43 0.43 0.42 0.42 18 0.34 0.33 0.33 0.32 0.32 19 1.90 0.18 0.17 0.17 0.17 0.17 20 0.13 0.13 0.12 0.12 0.12 21 0.81 0.06 0.06 0.06 0.06 0.06 22 0.05 0.04 0.04 0.04 0.04 23 0.35 0.02 0.02 0.02 0.02 0.02 24 0.01 0.01 0.01 0.01 0.01 25 0.19 0.01 0.01 0.01 0.01 0.01
TABLE IV
PEAKING PROCESS
M = 5.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 19.99 5.64 9.17 12.62 15.43 17.42 2 3.69 2.44 1.46 0.80 0.40 3 1.08 4.52 2.99 1.79 0.98 0.49 4 5.36 3.54 2.12 1.16 0.58 5 3.72 10.26 8.08 6.38 5.21 4.50 6 7.02 4.64 2.79 1.52 0.76 7 7.89 16.47 13.64 11.41 9.88 8.96 8 8.69 5.75 3.45 1.89 0.94 9 11.99 7.08 19.09 16.34 14.46 13.31 10 6.99 6.85 4.11 2.25 1.13 11 14.12 5.25 5.15 19.20 16.99 15.64 12 4.95 4.86 4.77 2.61 1.31 13 13.55 3.46 3.39 3.33 16.73 15.21 14 3.13 3.07 3.01 2.97 1.49 15 10.92 2.05 2.01 1.97 1.95 12.72 16 1.77 1.74 1.71 1.69 1.67 17 7.61 1.10 1.08 1.06 1.04 1.03 18 0.91 0.89 0.88 0.87 0.86 19 4.65 0.54 0.52 0.52 0.51 0.50 20 0.43 0.42 0.41 0.41 0.40 21 2.55 0.24 0.24 0.23 0.23 0.23 22 0.18 0.18 0.18 0.18 0.17 23 1.23 0.10 0.10 0.10 0.09 0.09 24 0.07 0.07 0.07 0.07 0.07 25 0.50 0.04 0.04 0.04 0.04 0.04 26 0.03 0.03 0.03 0.03 0.03 27 0.18 0.01 0.01 0.01 0.01 0.01
TABLE V
PEAKING PROCESS
M = 6.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized 1-Olefins of C x No. of Base and Above Isomerized C of Case C 10 C 12 C 14 C 16 C 18 Acid No and and and and and Product Peaking Above Above Above Above Above ____________________________________________________________ ______________ 1 17.73 3.22 5.65 8.51 11.32 13.69 2 3.43 2.59 1.79 1.14 0.67 3 0.43 4.21 3.17 2.20 1.39 0.82 4 4.98 3.76 2.60 1.65 0.97 5 1.77 7.66 6.22 4.85 3.73 2.92 6 6.53 4.93 3.41 2.17 1.27 7 4.55 12.14 10.28 8.51 7.05 6.00 8 8.08 6.10 4.22 2.68 1.57 9 8.15 7.21 15.34 13.16 11.36 10.05 10 7.36 7.27 5.03 3.19 1.87 11 11.53 6.10 6.02 17.47 15.32 13.76 12 6.00 5.92 5.83 3.71 2.17 13 13.26 4.64 4.58 4.51 17.61 15.81 14 4.40 4.34 4.28 4.22 2.47 15 12.86 3.19 3.15 3.10 3.06 15.69 16 2.92 2.88 2.84 2.80 2.77 17 10.71 2.00 1.97 1.94 1.92 1.90 18 1.77 1.74 1.72 1.69 1.68 19 7.92 1.15 1.13 1.11 1.10 1.09 20 0.98 0.97 0.95 0.94 0.93 21 5.15 0.61 0.60 0.59 0.58 0.57 22 0.50 0.49 0.49 0.48 0.47 23 3.13 0.30 0.29 0.29 0.28 0.28 24 0.24 0.23 0.23 0.23 0.22 25 1.62 0.13 0.13 0.13 0.13 0.13 26 0.10 0.10 0.10 0.10 0.10 27 0.79 0.06 0.06 0.06 0.05 0.05 28 0.04 0.04 0.04 0.04 0.04 29 0.34 0.02 0.02 0.02 0.02 0.02 30 0.02 0.02 0.02 0.02 0.02 31 0.18 0.01 0.01 0.01 0.01 0.01
TABLE VI
SUMMARY OF PEAKING PROCESS
M = 2-6
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ M= 2.00 1 35.29 21.53 25.01 26.40 26.86 27.00 2-4 13.57 6.90 2.07 0.55 0.13 0.03 5-9 44.18 68.24 69.66 64.78 63.40 63.06 10-15 6.76 3.27 3.20 8.22 9.54 9.85 16-19 0.18 0.04 0.04 0.04 0.04 0.04 20-30 0.00 0.00 0.00 0.00 0.00 0.00 M=3.00 1 27.42 14.98 19.59 22.29 23.64 24.21 2-4 6.26 11.00 4.74 1.83 0.63 0.20 5-9 44.61 64.07 65.99 56.79 52.96 51.55 10-15 19.79 9.45 9.18 18.60 22.27 23.54 16-19 1.74 0.46 0.44 0.44 0.44 0.44 20-30 0.19 0.03 0.03 0.03 0.03 0.03 M=4.00 1 22.94 9.50 13.97 17.44 19.72 21.01 2-4 2.65 13.25 7.32 3.64 1.65 0.68 5-9 34.92 57.42 59.40 48.05 41.84 38.81 10-15 32.29 17.75 17.32 28.90 34.85 37.57 16-19 5.88 1.78 1.72 1.71 1.68 1.67 20-30 1.35 0.28 0.27 0.26 0.26 0.26 M=5.00 1 19.99 5.64 9.17 12.62 15.43 17.42 2-4 1.09 13.57 8.97 5.37 2.94 1.47 5-9 23.60 49.52 51.20 40.37 32.96 28.47 10-15 38.59 25.83 25.33 36.39 43.50 47.50 16-19 12.26 4.32 4.23 4.17 4.11 4.06 20-30 4.46 1.10 1.09 1.07 1.06 1.04 M=6.00 1 17.73 3.22 5.65 8.51 11.32 13.69 2-4 0.43 12.62 9.52 6.59 4.18 2.46 5-9 14.37 41.62 42.87 34.15 26.99 21.81 10-15 37.65 31.69 31.28 40.22 47.11 51.77 16-19 18.63 7.84 7.72 7.61 7.51 7.44 20-30 11.21 3.01 2.96 2.93 2.88 2.84
TABLE VII
PEAKING PROCESS
M = 2.00
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 35.29 14.74 20.73 23.07 23.84 24.06 2 3.14 0.93 0.25 0.06 0.01 3 13.57 3.85 1.14 0.30 0.07 0.02 4 4.56 1.35 0.36 0.08 0.02 5 18.71 5.27 1.56 0.41 0.10 0.02 6 5.98 1.77 0.47 0.11 0.02 7 15.84 45.80 39.70 37.77 37.22 37.08 8 7.40 2.19 0.58 0.14 0.03 9 9.63 3.67 25.26 23.21 22.63 22.49 10 2.70 2.61 0.69 0.16 0.04 11 4.53 1.25 1.20 11.35 10.74 10.59 12 0.84 0.81 0.80 0.19 0.04 13 1.74 0.37 0.35 0.35 4.25 4.09 14 0.23 0.22 0.22 0.22 0.05 15 0.49 0.09 0.09 0.09 0.09 1.35 16 0.05 0.05 0.05 0.05 0.05 17 0.18 0.02 0.02 0.02 0.02 0.02
TABLE VIII
PEAKING PROCESS
M = 3.00
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 27.42 10.04 16.15 19.68 21.42 22.16 2 3.88 1.66 0.64 0.22 0.07 3 6.26 4.76 2.04 0.78 0.27 0.09 4 5.64 2.41 0.93 0.32 0.10 5 12.98 6.51 2.79 1.07 0.37 0.12 6 7.39 3.16 1.22 0.42 0.13 7 16.55 34.10 28.47 25.82 24.72 24.31 8 9.14 3.91 1.51 0.52 0.16 9 15.08 5.62 26.95 23.89 22.61 22.14 10 4.83 4.66 1.79 0.62 0.20 11 10.68 2.74 2.64 17.62 16.21 15.70 12 2.20 2.12 2.08 0.72 0.23 13 6.08 1.16 1.12 1.10 9.70 9.14 14 0.88 0.85 0.83 0.82 0.26 15 3.03 0.44 0.42 0.42 0.41 4.58 16 0.31 0.30 0.29 0.29 0.29 17 1.23 0.15 0.14 0.14 0.14 0.14 18 0.10 0.10 0.09 0.09 0.09 19 0.51 0.05 0.04 0.04 0.04 0.04 20 0.03 0.03 0.03 0.03 0.03 21 0.19 0.01 0.01 0.01 0.01 0.01
TABLE IX
PEAKING PROCESS
M = 4.00
Recycle = C 2 -6
1-Olefins of C x-2 and Below Not Isomerized No. of Base 1-olefins of C x C of Case and above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above 1 22.94 6.47 11.62 15.60 18.19 19.65 2 4.10 2.26 1.12 0.50 0.21 3 2.65 5.02 2.77 1.37 0.62 0.25 4 5.95 3.27 1.63 0.73 0.30 5 7.36 6.87 3.78 1.88 0.85 0.35 6 7.80 4.29 2.13 0.96 0.39 7 12.44 24.63 20.25 17.51 16.01 15.27 8 9.65 5.31 2.64 1.19 0.49 9 15.12 6.96 24.54 21.22 19.40 18.51 10 6.52 6.33 3.14 1.42 0.58 11 14.24 4.33 4.20 20.63 18.54 17.52 12 3.84 3.73 3.65 1.64 0.68 13 10.92 2.37 2.30 2.25 14.79 13.66 14 1.99 1.94 1.90 1.87 0.77 15 7.13 1.15 1.12 1.10 1.08 9.17 16 0.92 0.90 0.88 0.87 0.86 17 3.98 0.51 0.49 0.48 0.48 0.47 18 0.39 0.38 0.37 0.36 0.36 19 1.90 0.20 0.20 0.19 0.19 0.19 20 0.15 0.14 0.14 0.14 0.14 21 0.81 0.07 0.07 0.07 0.07 0.07 22 0.05 0.05 0.05 0.05 0.05 23 0.35 0.02 0.02 0.02 0.02 0.02 24 0.02 0.02 0.02 0.02 0.02 25 0.19 0.01 0.01 0.01 0.01 0.01
TABLE X
PEAKING PROCESS
M = 5.00
Recycle = C 2 -6
1Olefins of C x -2 and Below Not Isomerized No. of Base 1Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 19.99 3.99 7.78 11.47 14.47 16.58 2 3.92 2.59 1.55 0.85 0.42 3 1.09 4.81 3.18 1.90 1.04 0.52 4 5.70 3.76 2.25 1.23 0.62 5 3.72 6.58 4.35 2.60 1.42 0.71 6 7.47 4.93 2.96 1.61 0.81 7 7.89 17.51 14.48 12.10 10.48 9.49 8 9.24 6.10 3.66 2.00 1.00 9 11.99 7.52 20.27 17.34 15.33 14.10 10 7.43 7.27 4.36 2.38 1.19 11 14.12 5.58 5.46 20.37 18.01 16.57 12 5.27 5.16 5.06 2.76 1.38 13 13.55 3.68 3.60 3.54 17.73 16.11 14 3.33 3.26 3.19 3.15 1.58 15 10.92 2.18 2.13 2.09 2.06 13.48 16 1.89 1.85 1.81 1.79 1.77 17 7.61 1.17 1.14 1.12 1.10 1.09 18 0.97 0.95 0.93 0.92 0.91 19 4.65 0.57 0.56 0.55 0.54 0.53 20 0.46 0.45 0.44 0.43 0.43 21 2.55 0.26 0.25 0.25 0.24 0.24 22 0.20 0.19 0.19 0.19 0.18 23 1.23 0.11 0.10 0.10 0.10 0.10 24 0.08 0.08 0.08 0.07 0.07 25 0.50 0.04 0.04 0.04 0.04 0.04 26 0.03 0.03 0.03 0.03 0.03 27 0.18 0.01 0.01 0.01 0.01 0.01
TABLE XI
PEAKING PROCESS
M = 6.00
Recycle = C 2 -6
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C and and Above Above Above Above Above ____________________________________________________________ ______________ 1 17.73 2.41 4.91 7.87 10.76 13.20 2 3.53 2.66 1.84 1.17 0.68 3 0.43 4.33 3.26 2.26 1.43 0.84 4 5.12 3.86 2.67 1.70 0.99 5 1.77 5.92 4.47 3.09 1.96 1.15 6 6.72 5.07 3.50 2.22 1.30 7 4.45 12.48 10.57 8.74 7.25 6.16 8 8.31 6.27 4.33 2.75 1.61 9 8.15 7.42 15.78 13.52 11.67 10.32 10 7.58 7.47 5.17 3.28 1.92 11 11.53 6.28 6.19 17.65 15.74 14.14 12 6.17 6.09 6.00 3.81 2.23 13 13.26 4.77 4.71 4.64 18.09 16.24 14 4.52 4.46 4.40 4.34 2.54 15 12.86 3.28 3.24 3.19 3.15 16.11 16 3.00 2.96 2.92 2.88 2.85 17 10.71 2.06 2.03 2.00 1.97 1.95 18 1.82 1.79 1.76 1.74 1.72 19 7.92 1.18 1.16 1.15 1.13 1.12 20 1.01 0.99 0.98 0.96 0.95 21 5.15 0.62 0.61 0.60 0.60 0.59 22 0.51 0.51 0.50 0.49 0.49 23 3.13 0.30 0.30 0.30 0.29 0.29 24 0.24 0.24 0.24 0.23 0.23 25 1.62 0.14 0.14 0.13 0.13 0.13 26 0.11 0.11 0.10 0.10 0.10 27 0.79 0.06 0.06 0.06 0.06 0.06 28 0.04 0.04 0.04 0.04 0.04 29 0.34 0.02 0.02 0.02 0.02 0.02 30 0.02 0.02 0.02 0.02 0.02 31 0.18 0.01 0.01 0.01 0.01 0.01
TABLE XII
SUMMARY OF PEAKING PROCESS
M = 2-6
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ M= 2.00 1 35.29 14.74 20.73 23.07 23.84 24.06 2-5 32.28 16.82 4.98 1.32 0.31 0.07 6-10 25.47 65.55 71.53 62.72 60.26 59.66 11-15 6.76 2.78 2.67 12.81 15.49 16.12 16-20 0.18 0.07 0.07 0.07 0.07 0.07 21-30 0.00 0.00 0.00 0.00 0.00 0.00 M=3.00 1 27.42 10.04 16.15 19.68 21.42 22.16 2-5 19.24 20.79 8.90 3.42 1.18 0.38 6-10 31.63 61.08 67.15 54.23 48.89 46.94 11-15 19.79 7.42 7.15 22.05 27.86 29.91 16-20 1.74 0.64 0.61 0.59 0.59 0.59 21-30 0.19 0.01 0.01 0.01 0.01 0.01 M=4.00 1 22.94 6.47 11.62 15.60 18.19 19.65 2-5 10.01 21.94 12.08 6.00 2.70 1.11 6-10 27.56 55.56 60.72 46.64 38.98 35.24 11-15 32.29 13.68 13.29 29.53 37.92 41.80 16-20 5.88 2.17 2.11 2.06 2.04 2.02 21-30 1.35 0.17 0.17 0.17 0.17 0.17 M=5.00 1 19.99 3.99 7.78 11.47 14.47 16.58 2-5 4.81 21.01 13.88 8.30 4.54 2.27 6-10 19.88 49.17 53.05 40.42 31.80 26.59 11-15 38.59 20.04 19.61 34.25 43.71 49.12 16-20 12.26 5.05 4.95 4.85 4.78 4.73 21-30 4.46 0.73 0.70 0.70 0.68 0.67 M=6.00 1 17.73 2.41 4.91 7.87 10.76 13.20 2-5 2.20 18.90 14.25 9.86 6.26 3.66 6-10 12.60 42.51 45.16 35.26 27.17 21.31 11-15 37.65 25.02 24.69 36.18 45.13 51.26 16-20 18.63 9.07 8.93 8.81 8.68 8.59 21-30 11.21 2.07 2.06 2.02 1.99 1.98
TABLE XIII
SUMMARY OF PEAKING PROCESS
W/O RECYCLED OR ISOMERIZED
W/O isomerized for each case Where C x and above are isomerized W/O C 10 C 12 C 14 C 16 C 18 M- Recycled and and and and and Valve C 2 -4 C 2 -6 above Above Above Above Above ____________________________________________________________ ______________ 2.00 22.56 49.62 26.32 11.28 4.06 1.26 0.34 3.00 8.71 25.52 52.08 31.08 15.95 7.13 2.81 4.00 3.30 12.08 72.28 52.75 33.99 19.40 9.88 5.00 1.24 5.45 85.20 70.57 53.03 35.97 22.04 6.00 0.46 2.37 92.33 82.97 69.20 53.14 37.40
It can be seen from the data presented in these tables that the peaking process proposed has a high degree of versatility. The acids of various carbon number do not have the same value on the commercial market. Thus, the ranges of acids that will be selected fro peaking will be determined by the economics. The versatility offered by this peaking process would have a definite economic advantage. In general, the middle range of acids and/or aldehydes (C 5 -15 ) are more valuable than the lower (C 2 -4 ) or higher (C 16 -x ) ranges. The proposed peaking process allows the production of this middle range with much lower content of low range (encountered in isomerization of total olefin mixture) or high range (encountered in nonisomerized olefin mixture).
Although these calculations were based on a statistical distribution of the double bond at all possible positions on the carbon chain, this is an idealistic situation. In actual fact, most isomerization procedures produce a higher concentration of internal double bonds than would be expected from a statistical distribution. This is a favorable situation and would actually improve the proposed peaking process. Thus, the data presented here would be a minimum example of the peaking process.
This invention relates to oxidation of a mixture of alpha olefins so as to obtain oxidation products, such as aldehydes and carboxylic acids, having carbon atoms in a narrower range than did the original mixture.
It is known to produce alpha olefins in the prior art. It is known, for example, that alpha olefins can be prepared from organometal compounds such as aluminum trialkyls by olefin displacement, thermal displacement, or catalytic displacement. See for example U.S. Pat. Nos. 2,971,969, 3,344,202, and 3,280,023. It is also known that long-chain alpha olefins can be prepared by reacting ethylene in presence of catalytic amounts of metal alkyls; see British Pat. Nos. 1,020,563 and 1,037,866 and US Patents Nos. 2,699,457 and 3,322,844. It is also known to produce such alpha olefins by cracking paraffins. The prior art also teaches isomerizing alpha olefins to internal olefins; see U.S. Pat. Nos. 2,956,094, 3,217,061, 3,277,191, and 3,340,322.
It is also known that olefins can be oxidized to aldehydes and/or acids by several means such as ozonolysis, permanganate, chromic acid, osmium tetroxide, and the like.
It is also known in the prior art, see cited patents as examples, that the normal source of olefin production results in a statistical distribution of olefin chain lengths known as a Poisson distribution.
It is also known from the art cited that alpha olefins prepared from metal alkyls, particularly aluminum trialkyls, can be polymerized to various degrees; e.g., M-values, by controlling growth conditions such as temperature, pressure, and time. M-value means the average number of ethylenes added per alkyl substituent.
OBJECTS OF THIS INVENTION
It is an object of this invention to produce oxidized products from alpha olefins having carbon atoms varying over a wide range wherein the product will have carbon atoms varying over a substantially narrower range.
SUMMARY OF THE INVENTION
According to this invention, a mixture of alpha olefins is separated into at least two fractions, one fraction containing olefins having carbon atoms below a predetermined number and one fraction having carbon atoms of said predetermined number and more. At least one high molecular weight fraction, e.g., containing carbon atoms of the predetermined number and more, is isomerized to produce internal olefins preferably predominating in unsaturation near the center of the chain. The nonisomerized lower molecular weight fraction and the isomerized fraction are oxidized to the aldehyde and/or acid thereby producing product having carbon atoms predominately of intermediate chain length.
In this specification and claims, the terms high molecular weight and low molecular weight are relative only and mean that each fraction will consist of compounds containing at least a mixture of two materials of different number of carbon atoms.
BRIEF DESCRIPTION OF THE DRAWING
The drawing is a schematic flow diagram showing a preferred flow scheme for carrying out the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention can best be described by referring to the drawing. An alpha olefin supply 1 is passed to olefin separation zone 2 via conduit 5 wherein the olefins are separated into at least one low molecular weight fraction and at least one high molecular weight fraction. The total number of fractions and choice of separation points will be dependent upon the composition of the original mixture and the desired product. The separation can be any desired process; however, distillation will be generally used. The higher molecular weight fraction is passed via conduit 7 to isomerization zone 3 wherein the alpha olefins are isomerized to internal olefins by process already known. Any olefin fractions not desired to be oxidized are passed via conduit 6 to olefin storage or further processing, such as recycle to the growth reactor, as desired. It should be understood that conduit 6 can represent a plurality of conduits depending upon the number of cuts. The low molecular weight olefins from separation zone 2 pass via conduit 8 to preferably alpha olefin metathesis zone 11 wherein the alpha olefins are converted to internal olefins and ethylene according to the following formula: 2RCH = CH 2 ➝ RCH = CHR + CH 2 = CH 2 . The internal olefin is then separated from the ethylene and passed to oxidation zone 4 via conduit 12 while ethylene passes via conduit 13 to recycle or storage. The metathesis step is not a necessary step to the invention but has the advantage of avoiding the formation of formic acid. The isomerized olefins from zone 3 pass via conduit 9 to the oxidation zone 4. The olefins are oxidized by processes known forming aldehydes or acids depending upon known reaction conditions. The alpha olefins if zone 11 is omitted form C n -1 carboxylic acids or aldehydes and formic acid or formaldehyde. The internal olefins form a mixture of products breaking at the double bond.
As a specific example, a mixture of C 2 to C 30 alpha olefins obtained by displacement of aluminum alkyls is separated in separation zone 2 by distillation into a C 2 --C 4 fraction, a C 6 --C 12 fraction, and a C 14 to C 30 fraction. The C 2 --C 4 fraction is taken overhead via conduit 6 and is returned to the aluminum alkyl preparation for alkylation and further growth. The C 14 --C 30 fraction is passed to isomerization zone 3 via conduit 7 wherein it is isomerized. The effluent from zone 3 is passed along with the C 6 -12 fraction to the oxidation zone 4. A typical product distribution of such olefins having M-values of 4.00, 5.00, and 6.00 is given in Tables I, II, and III respectively. These results are summarized and shown in Table IV. For calculating olefin distribution for different M-values, see U.S. Pat. No. 3,344,202.
The process obviously can be varied to suit many particular needs. Some such modifications are described below. In all cases, it is assumed that there is a supply of C 2 --C 30 alpha olefins derived by ethylene growth of aluminum trialkyl having a typical statistical distribution.
Case 1: Assume a market for C 7 -15 carboxylic acids. The alpha olefins will be separated into three fractions; e.g., C 2 -6, C 8 -16, and C 18 -30. The C 2 -6 fraction is recycled and regrown, the C 18 -30 fraction is isomerized, and the C 8 -16 fraction and the isomerized fraction are oxidized resulting in an increase in the C 7 -15 desired carboxylic acids.
Case 2: Assume that the C 16 --C 18 olefins have greater value for some other purpose, e.g., olefin sulfonates, whereas the C 5 -13 acids and C 19 -21 acids have a market. The total olefins then will be separated into five fractions; e.g., C 2 -4 which is recycled and grown, C 6 -14 fraction is oxidized, C 16 -18 separated for sales, C 20 -22 fraction separately oxidized, and the C 24 -30 fraction isomerized and oxidized with the C 6 -14 fraction.
Case 3: Assume normal production of C 5 --C 15 acids; but, due to poor market conditions, the C 9 -11 acids are not moving. In this case, the olefins would be separated into five fractions with the C 2 -4 fraction being recycled to growth, the C 6 -8 fraction oxidized to acids, the C 10 -12 fraction would be recycled for growth or isomerized and oxidized with the C 6 -8 fraction depending upon demand, the C 18 -16 fraction oxidized, and the C 18 -30 fraction isomerized and oxidized with the C 14 -16 fraction.
It can be seen from the above modifications that by utilizing the variables, M-value, recycle and regrowth, and isomerization, the present invention offers a great deal of versatility in preparing oxidized products from a mixture of alpha olefins.
To show the effect of M-value and recycle on distribution, Tables I through V are presented to show carbon atom distribution on C 6 -30 alpha olefins at various M-values and recycle of C 2 -4 olefins. Table VI summarizes this data. Tables VII through XI show similar effect when C 2 -6 is recycled, whereas Table XII summarizes these tables. Table XIII shows a typical case where there is no recycle or isomerization at various M-values.
TABLE I
PEAKING PROCESS
M = 2.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and 1 35.29 21.53 25.01 26.40 26.86 27.00 2 1.88 0.56 0.15 0.04 0.01 3 13.57 2.30 0.69 0.18 0.04 0.01 4 2.72 0.82 0.22 0.05 0.01 5 18.71 30.73 27.94 27.04 26.78 26.71 6 3.57 1.07 0.29 0.07 0.01 7 15.84 27.33 24.04 22.98 22.68 22.61 8 4.42 1.32 0.35 0.08 0.02 9 9.63 2.19 15.29 14.12 13.79 13.71 10 1.61 1.58 0.42 0.10 0.02 11 4.53 0.74 0.73 6.91 6.55 6.46 12 0.50 0.49 0.49 0.12 0.02 13 1.74 0.22 0.21 0.21 2.59 2.49 14 0.14 0.13 0.13 0.13 0.03 15 0.49 0.06 0.06 0.06 0.05 0.83 16 0.03 0.03 0.03 0.03 0.03 17 0.18 0.01 0.01 0.01 0.01 0.01
TABLE II
PEAKING PROCESS
M = 3.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above 1 27.42 14.98 19.59 22.29 23.64 24.21 2 2.99 1.29 0.50 0.17 0.05 3 6.26 3.67 1.58 0.61 0.21 0.07 4 4.34 1.87 0.72 0.25 0.08 5 12.98 20.71 17.43 15.87 15.22 14.98 6 5.70 2.46 0.95 0.33 0.10 7 16.55 26.28 22.12 20.15 19.32 19.02 8 7.05 3.04 1.18 0.41 0.13 9 15.08 4.33 20.94 18.64 17.68 17.32 10 3.72 3.62 1.40 0.49 0.15 11 10.68 2.11 2.05 13.74 12.67 12.28 12 1.70 1.65 1.63 0.57 0.18 13 6.08 0.90 0.87 0.86 7.58 7.15 14 0.68 0.66 0.65 0.64 0.20 15 3.03 0.34 0.33 0.32 0.32 3.58 16 0.24 0.23 0.23 0.23 0.23 17 1.23 0.11 0.11 0.11 0.11 0.11 18 0.08 0.07 0.07 0.07 0.07 19 0.51 0.03 0.03 0.03 0.03 0.03 20 0.02 0.02 0.02 0.02 0.02 21 0.19 0.01 0.01 0.01 0.01 0.01
TABLE III
PEAKING PROCESS
M = 4.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 22.94 9.50 13.97 17.44 19.72 21.01 2 3.60 1.99 0.99 0.45 0.18 3 2.65 4.42 2.44 1.21 0.55 0.23 4 5.23 2.89 1.44 0.65 0.27 5 7.36 14.31 11.39 9.57 8.57 8.08 6 6.86 3.79 1.89 0.85 0.35 7 12.44 21.65 17.87 15.49 14.18 13.54 8 8.48 4.69 2.33 1.05 0.43 9 15.12 6.12 21.66 18.77 17.19 16.41 10 5.73 5.59 2.78 1.25 0.52 11 14.24 3.80 3.71 18.25 16.42 15.53 12 3.37 3.29 3.23 1.46 0.60 13 10.92 2.08 2.03 1.99 13.10 12.11 14 1.75 1.71 1.68 1.66 0.68 15 7.13 1.02 0.99 0.97 0.96 8.13 16 0.81 0.79 0.78 0.77 0.76 17 3.98 0.45 0.43 0.43 0.42 0.42 18 0.34 0.33 0.33 0.32 0.32 19 1.90 0.18 0.17 0.17 0.17 0.17 20 0.13 0.13 0.12 0.12 0.12 21 0.81 0.06 0.06 0.06 0.06 0.06 22 0.05 0.04 0.04 0.04 0.04 23 0.35 0.02 0.02 0.02 0.02 0.02 24 0.01 0.01 0.01 0.01 0.01 25 0.19 0.01 0.01 0.01 0.01 0.01
TABLE IV
PEAKING PROCESS
M = 5.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 19.99 5.64 9.17 12.62 15.43 17.42 2 3.69 2.44 1.46 0.80 0.40 3 1.08 4.52 2.99 1.79 0.98 0.49 4 5.36 3.54 2.12 1.16 0.58 5 3.72 10.26 8.08 6.38 5.21 4.50 6 7.02 4.64 2.79 1.52 0.76 7 7.89 16.47 13.64 11.41 9.88 8.96 8 8.69 5.75 3.45 1.89 0.94 9 11.99 7.08 19.09 16.34 14.46 13.31 10 6.99 6.85 4.11 2.25 1.13 11 14.12 5.25 5.15 19.20 16.99 15.64 12 4.95 4.86 4.77 2.61 1.31 13 13.55 3.46 3.39 3.33 16.73 15.21 14 3.13 3.07 3.01 2.97 1.49 15 10.92 2.05 2.01 1.97 1.95 12.72 16 1.77 1.74 1.71 1.69 1.67 17 7.61 1.10 1.08 1.06 1.04 1.03 18 0.91 0.89 0.88 0.87 0.86 19 4.65 0.54 0.52 0.52 0.51 0.50 20 0.43 0.42 0.41 0.41 0.40 21 2.55 0.24 0.24 0.23 0.23 0.23 22 0.18 0.18 0.18 0.18 0.17 23 1.23 0.10 0.10 0.10 0.09 0.09 24 0.07 0.07 0.07 0.07 0.07 25 0.50 0.04 0.04 0.04 0.04 0.04 26 0.03 0.03 0.03 0.03 0.03 27 0.18 0.01 0.01 0.01 0.01 0.01
TABLE V
PEAKING PROCESS
M = 6.00
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized 1-Olefins of C x No. of Base and Above Isomerized C of Case C 10 C 12 C 14 C 16 C 18 Acid No and and and and and Product Peaking Above Above Above Above Above ____________________________________________________________ ______________ 1 17.73 3.22 5.65 8.51 11.32 13.69 2 3.43 2.59 1.79 1.14 0.67 3 0.43 4.21 3.17 2.20 1.39 0.82 4 4.98 3.76 2.60 1.65 0.97 5 1.77 7.66 6.22 4.85 3.73 2.92 6 6.53 4.93 3.41 2.17 1.27 7 4.55 12.14 10.28 8.51 7.05 6.00 8 8.08 6.10 4.22 2.68 1.57 9 8.15 7.21 15.34 13.16 11.36 10.05 10 7.36 7.27 5.03 3.19 1.87 11 11.53 6.10 6.02 17.47 15.32 13.76 12 6.00 5.92 5.83 3.71 2.17 13 13.26 4.64 4.58 4.51 17.61 15.81 14 4.40 4.34 4.28 4.22 2.47 15 12.86 3.19 3.15 3.10 3.06 15.69 16 2.92 2.88 2.84 2.80 2.77 17 10.71 2.00 1.97 1.94 1.92 1.90 18 1.77 1.74 1.72 1.69 1.68 19 7.92 1.15 1.13 1.11 1.10 1.09 20 0.98 0.97 0.95 0.94 0.93 21 5.15 0.61 0.60 0.59 0.58 0.57 22 0.50 0.49 0.49 0.48 0.47 23 3.13 0.30 0.29 0.29 0.28 0.28 24 0.24 0.23 0.23 0.23 0.22 25 1.62 0.13 0.13 0.13 0.13 0.13 26 0.10 0.10 0.10 0.10 0.10 27 0.79 0.06 0.06 0.06 0.05 0.05 28 0.04 0.04 0.04 0.04 0.04 29 0.34 0.02 0.02 0.02 0.02 0.02 30 0.02 0.02 0.02 0.02 0.02 31 0.18 0.01 0.01 0.01 0.01 0.01
TABLE VI
SUMMARY OF PEAKING PROCESS
M = 2-6
Recycle = C 2 -4
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ M= 2.00 1 35.29 21.53 25.01 26.40 26.86 27.00 2-4 13.57 6.90 2.07 0.55 0.13 0.03 5-9 44.18 68.24 69.66 64.78 63.40 63.06 10-15 6.76 3.27 3.20 8.22 9.54 9.85 16-19 0.18 0.04 0.04 0.04 0.04 0.04 20-30 0.00 0.00 0.00 0.00 0.00 0.00 M=3.00 1 27.42 14.98 19.59 22.29 23.64 24.21 2-4 6.26 11.00 4.74 1.83 0.63 0.20 5-9 44.61 64.07 65.99 56.79 52.96 51.55 10-15 19.79 9.45 9.18 18.60 22.27 23.54 16-19 1.74 0.46 0.44 0.44 0.44 0.44 20-30 0.19 0.03 0.03 0.03 0.03 0.03 M=4.00 1 22.94 9.50 13.97 17.44 19.72 21.01 2-4 2.65 13.25 7.32 3.64 1.65 0.68 5-9 34.92 57.42 59.40 48.05 41.84 38.81 10-15 32.29 17.75 17.32 28.90 34.85 37.57 16-19 5.88 1.78 1.72 1.71 1.68 1.67 20-30 1.35 0.28 0.27 0.26 0.26 0.26 M=5.00 1 19.99 5.64 9.17 12.62 15.43 17.42 2-4 1.09 13.57 8.97 5.37 2.94 1.47 5-9 23.60 49.52 51.20 40.37 32.96 28.47 10-15 38.59 25.83 25.33 36.39 43.50 47.50 16-19 12.26 4.32 4.23 4.17 4.11 4.06 20-30 4.46 1.10 1.09 1.07 1.06 1.04 M=6.00 1 17.73 3.22 5.65 8.51 11.32 13.69 2-4 0.43 12.62 9.52 6.59 4.18 2.46 5-9 14.37 41.62 42.87 34.15 26.99 21.81 10-15 37.65 31.69 31.28 40.22 47.11 51.77 16-19 18.63 7.84 7.72 7.61 7.51 7.44 20-30 11.21 3.01 2.96 2.93 2.88 2.84
TABLE VII
PEAKING PROCESS
M = 2.00
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 35.29 14.74 20.73 23.07 23.84 24.06 2 3.14 0.93 0.25 0.06 0.01 3 13.57 3.85 1.14 0.30 0.07 0.02 4 4.56 1.35 0.36 0.08 0.02 5 18.71 5.27 1.56 0.41 0.10 0.02 6 5.98 1.77 0.47 0.11 0.02 7 15.84 45.80 39.70 37.77 37.22 37.08 8 7.40 2.19 0.58 0.14 0.03 9 9.63 3.67 25.26 23.21 22.63 22.49 10 2.70 2.61 0.69 0.16 0.04 11 4.53 1.25 1.20 11.35 10.74 10.59 12 0.84 0.81 0.80 0.19 0.04 13 1.74 0.37 0.35 0.35 4.25 4.09 14 0.23 0.22 0.22 0.22 0.05 15 0.49 0.09 0.09 0.09 0.09 1.35 16 0.05 0.05 0.05 0.05 0.05 17 0.18 0.02 0.02 0.02 0.02 0.02
TABLE VIII
PEAKING PROCESS
M = 3.00
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 27.42 10.04 16.15 19.68 21.42 22.16 2 3.88 1.66 0.64 0.22 0.07 3 6.26 4.76 2.04 0.78 0.27 0.09 4 5.64 2.41 0.93 0.32 0.10 5 12.98 6.51 2.79 1.07 0.37 0.12 6 7.39 3.16 1.22 0.42 0.13 7 16.55 34.10 28.47 25.82 24.72 24.31 8 9.14 3.91 1.51 0.52 0.16 9 15.08 5.62 26.95 23.89 22.61 22.14 10 4.83 4.66 1.79 0.62 0.20 11 10.68 2.74 2.64 17.62 16.21 15.70 12 2.20 2.12 2.08 0.72 0.23 13 6.08 1.16 1.12 1.10 9.70 9.14 14 0.88 0.85 0.83 0.82 0.26 15 3.03 0.44 0.42 0.42 0.41 4.58 16 0.31 0.30 0.29 0.29 0.29 17 1.23 0.15 0.14 0.14 0.14 0.14 18 0.10 0.10 0.09 0.09 0.09 19 0.51 0.05 0.04 0.04 0.04 0.04 20 0.03 0.03 0.03 0.03 0.03 21 0.19 0.01 0.01 0.01 0.01 0.01
TABLE IX
PEAKING PROCESS
M = 4.00
Recycle = C 2 -6
1-Olefins of C x-2 and Below Not Isomerized No. of Base 1-olefins of C x C of Case and above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above 1 22.94 6.47 11.62 15.60 18.19 19.65 2 4.10 2.26 1.12 0.50 0.21 3 2.65 5.02 2.77 1.37 0.62 0.25 4 5.95 3.27 1.63 0.73 0.30 5 7.36 6.87 3.78 1.88 0.85 0.35 6 7.80 4.29 2.13 0.96 0.39 7 12.44 24.63 20.25 17.51 16.01 15.27 8 9.65 5.31 2.64 1.19 0.49 9 15.12 6.96 24.54 21.22 19.40 18.51 10 6.52 6.33 3.14 1.42 0.58 11 14.24 4.33 4.20 20.63 18.54 17.52 12 3.84 3.73 3.65 1.64 0.68 13 10.92 2.37 2.30 2.25 14.79 13.66 14 1.99 1.94 1.90 1.87 0.77 15 7.13 1.15 1.12 1.10 1.08 9.17 16 0.92 0.90 0.88 0.87 0.86 17 3.98 0.51 0.49 0.48 0.48 0.47 18 0.39 0.38 0.37 0.36 0.36 19 1.90 0.20 0.20 0.19 0.19 0.19 20 0.15 0.14 0.14 0.14 0.14 21 0.81 0.07 0.07 0.07 0.07 0.07 22 0.05 0.05 0.05 0.05 0.05 23 0.35 0.02 0.02 0.02 0.02 0.02 24 0.02 0.02 0.02 0.02 0.02 25 0.19 0.01 0.01 0.01 0.01 0.01
TABLE X
PEAKING PROCESS
M = 5.00
Recycle = C 2 -6
1Olefins of C x -2 and Below Not Isomerized No. of Base 1Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ 1 19.99 3.99 7.78 11.47 14.47 16.58 2 3.92 2.59 1.55 0.85 0.42 3 1.09 4.81 3.18 1.90 1.04 0.52 4 5.70 3.76 2.25 1.23 0.62 5 3.72 6.58 4.35 2.60 1.42 0.71 6 7.47 4.93 2.96 1.61 0.81 7 7.89 17.51 14.48 12.10 10.48 9.49 8 9.24 6.10 3.66 2.00 1.00 9 11.99 7.52 20.27 17.34 15.33 14.10 10 7.43 7.27 4.36 2.38 1.19 11 14.12 5.58 5.46 20.37 18.01 16.57 12 5.27 5.16 5.06 2.76 1.38 13 13.55 3.68 3.60 3.54 17.73 16.11 14 3.33 3.26 3.19 3.15 1.58 15 10.92 2.18 2.13 2.09 2.06 13.48 16 1.89 1.85 1.81 1.79 1.77 17 7.61 1.17 1.14 1.12 1.10 1.09 18 0.97 0.95 0.93 0.92 0.91 19 4.65 0.57 0.56 0.55 0.54 0.53 20 0.46 0.45 0.44 0.43 0.43 21 2.55 0.26 0.25 0.25 0.24 0.24 22 0.20 0.19 0.19 0.19 0.18 23 1.23 0.11 0.10 0.10 0.10 0.10 24 0.08 0.08 0.08 0.07 0.07 25 0.50 0.04 0.04 0.04 0.04 0.04 26 0.03 0.03 0.03 0.03 0.03 27 0.18 0.01 0.01 0.01 0.01 0.01
TABLE XI
PEAKING PROCESS
M = 6.00
Recycle = C 2 -6
1-Olefins of C x -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C and and Above Above Above Above Above ____________________________________________________________ ______________ 1 17.73 2.41 4.91 7.87 10.76 13.20 2 3.53 2.66 1.84 1.17 0.68 3 0.43 4.33 3.26 2.26 1.43 0.84 4 5.12 3.86 2.67 1.70 0.99 5 1.77 5.92 4.47 3.09 1.96 1.15 6 6.72 5.07 3.50 2.22 1.30 7 4.45 12.48 10.57 8.74 7.25 6.16 8 8.31 6.27 4.33 2.75 1.61 9 8.15 7.42 15.78 13.52 11.67 10.32 10 7.58 7.47 5.17 3.28 1.92 11 11.53 6.28 6.19 17.65 15.74 14.14 12 6.17 6.09 6.00 3.81 2.23 13 13.26 4.77 4.71 4.64 18.09 16.24 14 4.52 4.46 4.40 4.34 2.54 15 12.86 3.28 3.24 3.19 3.15 16.11 16 3.00 2.96 2.92 2.88 2.85 17 10.71 2.06 2.03 2.00 1.97 1.95 18 1.82 1.79 1.76 1.74 1.72 19 7.92 1.18 1.16 1.15 1.13 1.12 20 1.01 0.99 0.98 0.96 0.95 21 5.15 0.62 0.61 0.60 0.60 0.59 22 0.51 0.51 0.50 0.49 0.49 23 3.13 0.30 0.30 0.30 0.29 0.29 24 0.24 0.24 0.24 0.23 0.23 25 1.62 0.14 0.14 0.13 0.13 0.13 26 0.11 0.11 0.10 0.10 0.10 27 0.79 0.06 0.06 0.06 0.06 0.06 28 0.04 0.04 0.04 0.04 0.04 29 0.34 0.02 0.02 0.02 0.02 0.02 30 0.02 0.02 0.02 0.02 0.02 31 0.18 0.01 0.01 0.01 0.01 0.01
TABLE XII
SUMMARY OF PEAKING PROCESS
M = 2-6
Recycle = C 2 -6
1-Olefins of C X -2 and Below Not Isomerized No. of Base 1-Olefins of C x C of Case and Above Isomerized Acid No C 10 C 12 C 14 C 16 C 18 Product Peaking and and and and and Above Above Above Above Above ____________________________________________________________ ______________ M= 2.00 1 35.29 14.74 20.73 23.07 23.84 24.06 2-5 32.28 16.82 4.98 1.32 0.31 0.07 6-10 25.47 65.55 71.53 62.72 60.26 59.66 11-15 6.76 2.78 2.67 12.81 15.49 16.12 16-20 0.18 0.07 0.07 0.07 0.07 0.07 21-30 0.00 0.00 0.00 0.00 0.00 0.00 M=3.00 1 27.42 10.04 16.15 19.68 21.42 22.16 2-5 19.24 20.79 8.90 3.42 1.18 0.38 6-10 31.63 61.08 67.15 54.23 48.89 46.94 11-15 19.79 7.42 7.15 22.05 27.86 29.91 16-20 1.74 0.64 0.61 0.59 0.59 0.59 21-30 0.19 0.01 0.01 0.01 0.01 0.01 M=4.00 1 22.94 6.47 11.62 15.60 18.19 19.65 2-5 10.01 21.94 12.08 6.00 2.70 1.11 6-10 27.56 55.56 60.72 46.64 38.98 35.24 11-15 32.29 13.68 13.29 29.53 37.92 41.80 16-20 5.88 2.17 2.11 2.06 2.04 2.02 21-30 1.35 0.17 0.17 0.17 0.17 0.17 M=5.00 1 19.99 3.99 7.78 11.47 14.47 16.58 2-5 4.81 21.01 13.88 8.30 4.54 2.27 6-10 19.88 49.17 53.05 40.42 31.80 26.59 11-15 38.59 20.04 19.61 34.25 43.71 49.12 16-20 12.26 5.05 4.95 4.85 4.78 4.73 21-30 4.46 0.73 0.70 0.70 0.68 0.67 M=6.00 1 17.73 2.41 4.91 7.87 10.76 13.20 2-5 2.20 18.90 14.25 9.86 6.26 3.66 6-10 12.60 42.51 45.16 35.26 27.17 21.31 11-15 37.65 25.02 24.69 36.18 45.13 51.26 16-20 18.63 9.07 8.93 8.81 8.68 8.59 21-30 11.21 2.07 2.06 2.02 1.99 1.98
TABLE XIII
SUMMARY OF PEAKING PROCESS
W/O RECYCLED OR ISOMERIZED
W/O isomerized for each case Where C x and above are isomerized W/O C 10 C 12 C 14 C 16 C 18 M- Recycled and and and and and Valve C 2 -4 C 2 -6 above Above Above Above Above ____________________________________________________________ ______________ 2.00 22.56 49.62 26.32 11.28 4.06 1.26 0.34 3.00 8.71 25.52 52.08 31.08 15.95 7.13 2.81 4.00 3.30 12.08 72.28 52.75 33.99 19.40 9.88 5.00 1.24 5.45 85.20 70.57 53.03 35.97 22.04 6.00 0.46 2.37 92.33 82.97 69.20 53.14 37.40
It can be seen from the data presented in these tables that the peaking process proposed has a high degree of versatility. The acids of various carbon number do not have the same value on the commercial market. Thus, the ranges of acids that will be selected fro peaking will be determined by the economics. The versatility offered by this peaking process would have a definite economic advantage. In general, the middle range of acids and/or aldehydes (C 5 -15 ) are more valuable than the lower (C 2 -4 ) or higher (C 16 -x ) ranges. The proposed peaking process allows the production of this middle range with much lower content of low range (encountered in isomerization of total olefin mixture) or high range (encountered in nonisomerized olefin mixture).
Although these calculations were based on a statistical distribution of the double bond at all possible positions on the carbon chain, this is an idealistic situation. In actual fact, most isomerization procedures produce a higher concentration of internal double bonds than would be expected from a statistical distribution. This is a favorable situation and would actually improve the proposed peaking process. Thus, the data presented here would be a minimum example of the peaking process.