C07C9/22

CATALYTIC UPCYCLING OF POLYOLEFINS VIA VERSATILE ALKYLALUMINUMS
20220213007 · 2022-07-07 ·

Disclosed herein is a process for the conversion of polymers, oligomers, or mixtures thereof into shorter alkanes, carboxylic acids, alcohols, alkyl halides or aldehydes. This process includes contacting the polymers, oligomers, or mixtures thereof with the compound of formula (I):


Al(R.sup.1).sub.3  (I)

where R.sup.1 is independently selected at each occurrence thereof from the group consisting of H, aryl, C.sub.1-C.sub.8 alkyl, and C.sub.1-C.sub.8 alkoxy, as a reaction mixture, in the presence of a catalyst selected from the group consisting of a transition metal catalyst, a lanthanide series metal catalyst, or combinations thereof.

Method and catalyst for selective oligomerization of ethylene

The present disclosure provides a method and a catalyst for selective oligomerization of ethylene. The raw material for the catalyst consists of a dehydropyridine annulene-type ligand, a transition metal compound, and an organometallic compound in a molar ratio of 1:0.5-100:0.1-5000. The present disclosure also provides a method for selective oligomerization of ethylene accomplished by using the above-mentioned catalyst. The catalyst for selective oligomerization of ethylene has high catalytic activity, high selectivity for the target products 1-hexene and 1-octene, and low selectivity for 1-butene and 1-C.sub.10.sup.+.

Method and catalyst for selective oligomerization of ethylene

The present disclosure provides a method and a catalyst for selective oligomerization of ethylene. The raw material for the catalyst consists of a dehydropyridine annulene-type ligand, a transition metal compound, and an organometallic compound in a molar ratio of 1:0.5-100:0.1-5000. The present disclosure also provides a method for selective oligomerization of ethylene accomplished by using the above-mentioned catalyst. The catalyst for selective oligomerization of ethylene has high catalytic activity, high selectivity for the target products 1-hexene and 1-octene, and low selectivity for 1-butene and 1-C.sub.10.sup.+.

Method for preparing paraffin

The present invention relates to a method for preparing paraffin, and can provide a method for preparing paraffin including a hydrogenation step of by-products of a process for preparing linear alpha olefins. Since the method for preparing paraffin of the present invention can convert the by-products of the process for preparing linear alpha olefins to paraffin at a high conversion ratio, it is possible to increase the added value of the by-products.

Method for preparing paraffin

The present invention relates to a method for preparing paraffin, and can provide a method for preparing paraffin including a hydrogenation step of by-products of a process for preparing linear alpha olefins. Since the method for preparing paraffin of the present invention can convert the by-products of the process for preparing linear alpha olefins to paraffin at a high conversion ratio, it is possible to increase the added value of the by-products.

Trialkylphosphonium ionic liquids, methods of making, and alkylation processes using trialkylphosphonium ionic liquids

A trialkylphosphonium haloaluminate compound having a formula: ##STR00001##
where R.sup.1, R.sup.2, and R.sup.3 are the same or different and each is independently selected from C.sub.1 to C.sub.8 hydrocarbyl; and X is selected from F, Cl, Br, I, or combinations thereof is described. An ionic liquid catalyst composition incorporating the trialkylphosphonium haloaluminate compound, methods of making the trialkylphosphonium haloaluminate compound, and alkylation processes incorporating the trialkylphosphonium haloaluminate compound are also described.

Trialkylphosphonium ionic liquids, methods of making, and alkylation processes using trialkylphosphonium ionic liquids

A trialkylphosphonium haloaluminate compound having a formula: ##STR00001##
where R.sup.1, R.sup.2, and R.sup.3 are the same or different and each is independently selected from C.sub.1 to C.sub.8 hydrocarbyl; and X is selected from F, Cl, Br, I, or combinations thereof is described. An ionic liquid catalyst composition incorporating the trialkylphosphonium haloaluminate compound, methods of making the trialkylphosphonium haloaluminate compound, and alkylation processes incorporating the trialkylphosphonium haloaluminate compound are also described.

Trialkylphosphonium ionic liquids, methods of making, and alkylation processes using trialkylphosphonium ionic liquids

A trialkylphosphonium haloaluminate compound having a formula: ##STR00001##
where R.sup.1, R.sup.2, and R.sup.3 are the same or different and each is independently selected from C.sub.1 to C.sub.8 hydrocarbyl; and X is selected from F, Cl, Br, I, or combinations thereof is described. An ionic liquid catalyst composition incorporating the trialkylphosphonium haloaluminate compound, methods of making the trialkylphosphonium haloaluminate compound, and alkylation processes incorporating the trialkylphosphonium haloaluminate compound are also described.

Even carbon number paraffin composition and method of manufacturing same

Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.

Even carbon number paraffin composition and method of manufacturing same

Paraffin compositions including mainly even carbon number paraffins, and a method for manufacturing the same, is disclosed herein. In one embodiment, the method involves contacting naturally occurring fatty acid/glycerides with hydrogen in a slurry bubble column reactor containing bimetallic catalysts with equivalent particle diameters from about 10 to about 400 micron. The even carbon number compositions are particularly useful as phase change material.