Methods for making linear internal olefins from mixtures of linear and branched olefins
US-2024051900-A1 · Feb 15, 2024 · US
US2016355451A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016355451-A1 |
| Application number | US-201515116908-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 5, 2015 |
| Priority date | Feb 7, 2014 |
| Publication date | Dec 8, 2016 |
| Grant date | — |
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A process for the preparation of a chemical composition comprising an aromatic compound α in a concentration B by weight, based on the total weight of the chemical composition, includes: a. providing the following reaction components: i. a chemical composition comprising the following: a) The aromatic compound α in a concentration A by weight based on the total weight of the chemical composition, and b) An olefin in an amount of about 50 to about 99.99 wt. %, based on the total weight of the chemical composition, and ii. an acid; and b. reacting the components to obtain the chemical composition comprising the aromatic compound α in a concentration B by weight based on the total weight of the chemical composition; wherein the concentration B is less than the concentration A.
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1 . A process for the preparation of a chemical composition comprising an aromatic compound α in a concentration B by weight, based on the total weight of the chemical composition, comprising: a. providing the following reaction components: i. a chemical composition comprising the following: a) The aromatic compound α in a concentration A by weight based on the total weight of the chemical composition, and b) An olefin in an amount in an amount of about 50 to about 99.99 wt. %, based on the total weight of the chemical composition, and ii. An acid selected from an acidic ionic liquid, a protic compound, an ammonium, an imidazolium, an anion selected from AlCl 4 − , AlBr 4 − , AlI 4 − , BF 4 − , PF 6 − , CF 3 SO 3 − , [(CF 3 SO 2 ) 2 N] − , toslyate, or a combination comprising at least one of the foregoing, or a combination comprising at least one of the foregoing; and b. reacting the components to obtain the chemical composition comprising the aromatic compound α in a concentration B by weight based on the total weight of the chemical composition; wherein the concentration B is less than the concentration A. 2 . The process according to claim 1 , wherein the olefin b) is an α-olefin, comprising a C 2 -C 20 olefin. 3 . (canceled) 4 . The process according to claim 1 , wherein the concentration A is about 2 ppm to about 10 wt. % based on the total weight of the chemical composition i. 5 . The process according to claim 1 , wherein the ratio of concentration A: concentration B is about 1:0 to about 1:0.1. 6 . The process according to claim 1 , wherein the aromatic compound is benzene. 7 . The process according to claim 1 , wherein a further olefin is present as a component of a), wherein the further olefin is different to the olefin b). 8 . The process according to claim 7 , wherein the further olefin is a C 2 -C 20 olefin. 9 . The process according to claim 1 , wherein the acid comprises an acidic ionic liquid or wherein the acid comprises a protic compound. 10 . (canceled) 11 . The process according to claim 1 , wherein the acid comprises an ammonium. 12 . The process according to claim 11 , wherein the ammonium has the general formula NR 4 , wherein R is hydrocarbon or hydrogen, and wherein each R can be the same as or different to the other R in the molecule. 13 . (canceled) 14 . The process according to claim 1 , wherein the acid comprises an imidazolium. 15 . The process according to claim 14 , wherein the imidazolium has the general formula wherein R 2 is alkyl; wherein each of R 1 , R 3 , R 4 is hydrocarbon or hydrogen; and wherein R 1 , R 2 , R 3 , R 4 within a molecule can be the same as or different to each other. 16 . (canceled) 17 . The process according to claim 15 , wherein R 2 is butyl and R 1 , R 2 and R 3 have one of the following configurations: a. R 1 , R 3 and R 4 are hydrogen; b. R 1 and R 3 are hydrogen and R 4 is alkyl; c. R 1 and R 4 are hydrogen and R 3 is alkyl; and d. R 4 and R 3 are hydrogen and R 1 is alkyl. 18 . The process according to claim 1 , wherein the acid comprises an anion selected from AlCl 4 − , AlBr 4 − , AlI 4 − , BF 4 − , PF 6 − , CF 3 SO 3 − , [(CF 3 SO 2 ) 2 N] − , tosylate, or a combination comprising at least one of the foregoing. 19 . The process according to claim 1 , wherein the acid is present in step b. in a concentration of about 0.1 to about 50 wt. %, based on the total weight of the reaction components. 20 . (canceled) 21 . The process according to claim 1 , wherein the chemical composition i. is a homogeneous liquid. 22 . The process according to claim 1 , wherein the reaction b. is carried out at a temperature of about 0 to about 250° C. 23 . A process for the preparation of a downstream product comprising: i. preparation of an alkene by a process according to claim 1 ; and ii. reaction of the alkene to form the downstream product. 24 . The process according to claim 23 , wherein the downstream product is a polymer. 25 . The process according to claim 23 , wherein the downstream product is a polythene or a polypropene. 26 . (canceled)
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