US3696134A - Process for peaking the oxidation products of 1-olefins - Google Patents
Process for peaking the oxidation products of 1-olefins Download PDFInfo
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- US3696134A US3696134A US1655A US3696134DA US3696134A US 3696134 A US3696134 A US 3696134A US 1655 A US1655 A US 1655A US 3696134D A US3696134D A US 3696134DA US 3696134 A US3696134 A US 3696134A
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- 238000000034 method Methods 0.000 title claims abstract description 41
- 230000003647 oxidation Effects 0.000 title description 9
- 238000007254 oxidation reaction Methods 0.000 title description 9
- 239000004711 α-olefin Substances 0.000 claims abstract description 35
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 150000001336 alkenes Chemical class 0.000 claims description 27
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 238000006073 displacement reaction Methods 0.000 claims description 6
- -1 carbon atom olefins Chemical class 0.000 claims description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 2
- 239000000047 product Substances 0.000 abstract description 30
- 239000000203 mixture Substances 0.000 abstract description 16
- 238000006317 isomerization reaction Methods 0.000 abstract description 9
- 150000001735 carboxylic acids Chemical class 0.000 abstract description 6
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 3
- 239000002184 metal Substances 0.000 abstract description 3
- 239000012467 final product Substances 0.000 abstract description 2
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 24
- 150000007513 acids Chemical class 0.000 description 11
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 11
- 238000009826 distribution Methods 0.000 description 9
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 8
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000005649 metathesis reaction Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241001647090 Ponca Species 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- UZUODNWWWUQRIR-UHFFFAOYSA-L disodium;3-aminonaphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].C1=CC=C(S([O-])(=O)=O)C2=CC(N)=CC(S([O-])(=O)=O)=C21 UZUODNWWWUQRIR-UHFFFAOYSA-L 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012285 osmium tetroxide Substances 0.000 description 1
- 229910000489 osmium tetroxide Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000005949 ozonolysis reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/28—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/126—Acids containing more than four carbon atoms
Definitions
- 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 nonisomerize'd 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.
- An alpha olefin supply 1 is passed to olefin 0 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.
- 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 alphaolefin metathesis zone 1 1 wherein the alpha olefins are converted to internal olefins and ethylene according to the following formula: 2RCH CH RCH CHR CH CH
- 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 1 1 is omitted form C carboxylic acids or aldehydes and formic acid or formaldehyde.
- the internal olefins form a mixture of products breaking at the double bond.
- a mixture of C to C alpha olefins obtained by displacement of aluminum alkyls is separated in separation zone 2 by distillation into a C -C fraction, a C C fraction, and a C to C fraction.
- the C -C fraction is taken overhead via conduit 6 and is returned to the aluminum alkyl preparation for alkylation and further growth.
- the C C 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 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.
- Case 1 Assume a market for C carboxylic acids. The alpha olefins will be separated into three fractions;
- the C24 fraction is recycled and regrown, the C fraction is isomerized, and the C fraction and the isomerized fraction are oxidized resulting in an increase in the C desired carboxylic acids.
- Case 2 Assume that the C C olefins have greater value for some other purpose, e.g., olefin sulfonates, whereas the C acids and C1921 acids have a market. The total olefins then will be separated into five fractions; e.g., C which is recycled and grown, C fraction is oxidized, C separated for sales, C 22 fraction separately oxidized, and the C2440 fraction isomerized and oxidized with the C fraction.
- C which is recycled and grown C fraction is oxidized
- C separated for sales C 22 fraction separately oxidized
- the C2440 fraction isomerized and oxidized with the C fraction.
- Case 3 Assume normal production of C -C acids; but, due to poor market conditions, the C acids are not moving. In this case, the olefins would be separated into five fractions with the C fraction being recycled to growth, the C fraction oxidized to acids, the C1042 fraction would be recycled for growth or isomerized and oxidized with the C fraction depending upon demand, the Clans fraction oxidized, and the C1840 fraction isomerized and oxidized with the C1446 fraction.
- Tables I through V are presented to show carbon atom distribution on C alpha olefins at various M-values and recycle of C olefins.
- Table VI summarizes this data.
- Tables V11 through X1 show similar effect when C is recycled, whereas Table XII summarizes these tables.
- Table Xlll shows a typical case where there is no recycle or isomerization at various M- values.
- a peaking process for preparing oxidized products selected from the group consisting of aldehydes and acids from a mixture of alpha olefins comprising separating said alpha olefms 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.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
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.
Description
United States Patent Washecheck [54] PROCESS FOR PEAKING THE OXIDATION PRODUCTS OF l-OLEFINS [72] .lnventor: Paul H. Washecheck, Ponca City,
91291756 1...- V [73] Assignee: Continental Oil Company, Ponca City, Okla. [22] Filed: Jan.9,1970
[21] Appl. No.: 1,655
Pattison, Fatty Acids and Their Industrial Applications Marcel Dekker, Inc., New York, 1968 pp. 363- 364.
[451 Oct. 3, 1972 Primary Examiner-Lewis Gotts Assistant Examiner-Ethel G. Love Attorney-Joseph C. Kotarski, Henry H. Huth, Robert B. Coleman, Jr. and Carroll Palmer [57] ABSTRACT 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 C,, product and C 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 metalalkyl growth product, M-values also have an influence on the final product.
6 Claims, 1 Drawing Figure o.- QLEFIN RECYCLE l3 TO GROWTH REACTOR ETHYLENE on STORAGE u.-OLEFIN 5 o.-OLEF IN 8 w-OLEFIN OLEFIN TO PRODUCT SUPPLY SEPARATION METATHESIS OXIDATION lL'OLEFlN ISOMERIZATION PROCESS FOR PEAKING THE OXIDATION PRODUCTS OF l-OLEFINS 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 producealpha olefins in the prior art.
It is known, for example, that alpha olefins can be 1 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. t
It isvalso 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 nonisomerize'd 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 0 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 alphaolefin metathesis zone 1 1 wherein the alpha olefins are converted to internal olefins and ethylene according to the following formula: 2RCH CH RCH CHR CH CH 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 1 1 is omitted form C carboxylic acids or aldehydes and formic acid or formaldehyde. The internal olefins form a mixture of products breaking at the double bond.
Asa specific example, a mixture of C to C alpha olefins obtained by displacement of aluminum alkyls is separated in separation zone 2 by distillation into a C -C fraction, a C C fraction, and a C to C fraction. The C -C fraction is taken overhead via conduit 6 and is returned to the aluminum alkyl preparation for alkylation and further growth. The C C 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 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 --C alpha olefins derived by ethylene growth of aluminum trialkyl having a typical statistical distribution.
Case 1: Assume a market for C carboxylic acids. The alpha olefins will be separated into three fractions;
e.g., C243, C348. and C1g.3o The C24 fraction is recycled and regrown, the C fraction is isomerized, and the C fraction and the isomerized fraction are oxidized resulting in an increase in the C desired carboxylic acids.
Case 2: Assume that the C C olefins have greater value for some other purpose, e.g., olefin sulfonates, whereas the C acids and C1921 acids have a market. The total olefins then will be separated into five fractions; e.g., C which is recycled and grown, C fraction is oxidized, C separated for sales, C 22 fraction separately oxidized, and the C2440 fraction isomerized and oxidized with the C fraction.
Case 3: Assume normal production of C -C acids; but, due to poor market conditions, the C acids are not moving. In this case, the olefins would be separated into five fractions with the C fraction being recycled to growth, the C fraction oxidized to acids, the C1042 fraction would be recycled for growth or isomerized and oxidized with the C fraction depending upon demand, the Clans fraction oxidized, and the C1840 fraction isomerized and oxidized with the C1446 fraction.
It can be seen from the above modifications that by utilizing the variables, M-value, recycle and regrowth, and isomerization, the present invention offei's 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 alpha olefins at various M-values and recycle of C olefins. Table VI summarizes this data. Tables V11 through X1 show similar effect when C is recycled, whereas Table XII summarizes these tables. Table Xlll shows a typical case where there is no recycle or isomerization at various M- values.
TABLE 1 PEAKING PROCESS Recycle C l-Olefins of C and Below Not lsomerized No. of Base l-Olefins of C C of Case and Above lsomerized Acid No C C C C C 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
TABLE 11 PEAKING PROCESS Recycle C 5,
1-O1ei'ms of C and Below Not isomerized No. of Base l-Olefins of C C of Case and Above lsomerized Acid No C C C C C 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 111 PEAKING PROCESS Recycle C l-Olefins of C and Below Not lsomerized No. of Base l-Oleflns of C, C of Case and Above lsomerized Acid No C C C C C Product Peaking and and and and and Above Above Above Above Above 5 TABLE IV PEAKING PROCESS Recycle C 3,
l-Olefins of C and Below Not lsomerized N0. of Base l-Olefins of C C of Case and Above lsomerized Acid N m 12 u m m Product Peaking and and and and and Above Above Above Above Above TABLE V PEAKING PROCESS Recycle C l-Olefins o1"C, and Below N01 lsomerized l-()1e1'lns 01' C No. of Base and Above lsomerizcd C 01 Case C C, C, C C Acid No and and and andand Product Peaking Above Above Above AboveAbove TABLE VI SUMMARY OF PEAKING PROCESS Recycle C 1-O1efins of C 2, and Below Not lsomerized No. of Base l-Olefins of C C of Case and Above Isomerized Acid N9 10 12 u m m Product Peaking and and and and and Above Above Above Above Above TABLE V11 PEAKlNG PROCESS Recycle C l-Olefins of C and Below Not lsomerized No. of Base l-Olefins of C, C of Case and Above lsomerized Acid No C C C C C Product Peaking and and and and and Above Above Above Above Above TABLE V111 PEAKING PROCESS Recycle C 1-Olefins of C and Below No! lsomerized No. of Base 1-Olefins of C C of Case and above lsomerized Acid No C C C C C Produci Peaking and and and and and Above Above Above Above Above TABLE lX PEAKING PROCESS Recycle C l-Olefins of C 2 and Below Not lsomerized N0. of Base l-olefins of C C of Case and above lsomerized Acid N0 C10 12 u m m 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 Recycle C 10lefins of C and Below Not lsomerized No. of Base 101efins of C, C of Case and Above lsomerized Acid No C C C C, C, Product Peaking and and and and and Above Above Above Above Above TABLE X1 PEAKING PROCESS Recycle C 1-Olefins of C and Below No! lsomerized No. of Base l-Olefins of C C of Case and Above lsomerized Acid N0 and Above Above Above Above Above TABLE XII SUMMARY OF PEAKING PROCESS Recycle C 1-Olefins of C and Below Not lsomerized No. of Base l-Olefins of C C of Case and Above lsomerized Acid No C C C, C C 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 2-5 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 ll-l5 19.79 7.42 7.15 22.05 27.86 29.91 1620 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
TABLE X111 SUMMARY OF PEAKING PROCESS W/O RECYCLED OR ISOMERIZED W/O isomerized for each case Where C, and above are isomerized W C12 CH w m M- Recycled and and and and and Valve C C above Above Above Above Above 1t 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 are more valuable than the lower (C or higher (C 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.
Having thus described the invention, 1 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 olefms 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-l.
6. The process of claim 5 wherein the low molecular weight fraction to be oxidized consists of C to C alpha olefins and the higher molecular eight fraction consists of C to C alpha olefins.
1 j "UNITED STATES' PA'TEN T OFFICE CERTIFICATE OF 'CORRECTIUN. 1 Petent- No; 1 3,696,134 ate; October 5]; 19 72 I Inventofls) WaShe check It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Page column 3, line 23', "0 4 should read -+-C r nd" insert ----Above-z--- Page 4, column 3 line 53, in the last five columns" or TABLE 1., a;
, Page 6,"'ee1umn 8, in the'headi-ng of'TABLE x1, 601m 1, after "Acid" insert '--Product-- F Page 6, column 8 inane heading of- TABLE XI, column-2, after, "No" insert --Pead :ing---.
Page 6, column 8, in the heading of TABLE XI, column 3, after Y "C" insert ---i' 'en'dt Page 6, column 8, in the heading of TABLE XI, column' t before "Above" insert C aund---- I Pa e 6, column 8, in the heading of TABLE XI, column 5, before Above insert --C land-'-. I v
Page 6, column 8., in the heading ofTABLE XI, 'oolumn 6,, before 1Above insert C and". 6
Page 6, column 8, in the heading of TABLE XI, column 7', before "and" insert -'---C V Page 7-, column 9, line 51, "fro" should 'read -}-for-'-.
It is certified that eri'or appear 1n the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Signed and sealed this 20th day of February 1973..
(SEAL) Attest:
EDWARD M.FLETCHER,JR. ROBERT GOTTSCHALK r Commissioner of Patents Atcesting Officer
Claims (5)
- 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.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US165570A | 1970-01-09 | 1970-01-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3696134A true US3696134A (en) | 1972-10-03 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US1655A Expired - Lifetime US3696134A (en) | 1970-01-09 | 1970-01-09 | Process for peaking the oxidation products of 1-olefins |
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| Country | Link |
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| US (1) | US3696134A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4029682A (en) * | 1974-12-23 | 1977-06-14 | Emery Industries, Inc. | Soaps and ester-soaps of α-olefin derived high molecular weight acids |
| US4038297A (en) * | 1973-05-17 | 1977-07-26 | Emery Industries, Inc. | High molecular weight monocarboxylic acids and ozonization process for their preparation |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US25797A (en) * | 1859-10-18 | Improvement in harvesters | ||
| US3250757A (en) * | 1961-05-18 | 1966-05-10 | Phillips Petroleum Co | Method and apparatus for controlling feed to a polymerization reaction |
| US3369037A (en) * | 1964-04-29 | 1968-02-13 | Ethyl Corp | Preparation of high purity primary organo aluminum compounds |
| US3557169A (en) * | 1968-10-29 | 1971-01-19 | Ethyl Corp | Process for producing carboxylic acids |
-
1970
- 1970-01-09 US US1655A patent/US3696134A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US25797A (en) * | 1859-10-18 | Improvement in harvesters | ||
| US3250757A (en) * | 1961-05-18 | 1966-05-10 | Phillips Petroleum Co | Method and apparatus for controlling feed to a polymerization reaction |
| US3369037A (en) * | 1964-04-29 | 1968-02-13 | Ethyl Corp | Preparation of high purity primary organo aluminum compounds |
| US3557169A (en) * | 1968-10-29 | 1971-01-19 | Ethyl Corp | Process for producing carboxylic acids |
Non-Patent Citations (1)
| Title |
|---|
| Pattison, Fatty Acids and Their Industrial Applications Marcel Dekker, Inc., New York, 1968 pp. 363 364. * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4038297A (en) * | 1973-05-17 | 1977-07-26 | Emery Industries, Inc. | High molecular weight monocarboxylic acids and ozonization process for their preparation |
| US4029682A (en) * | 1974-12-23 | 1977-06-14 | Emery Industries, Inc. | Soaps and ester-soaps of α-olefin derived high molecular weight acids |
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