C07C9/22

Catalysts for the deoxygenation of esters of free fatty acids and triglycerides

It is provided solid, heterogeneous catalysts for the deoxygenation of esters of free fatty acids and triglycerides, and for the production of hydrocarbons that can be used as biofuels. More particularly, the catalyst comprises at least one metal oxide, the catalyst having a formula Al.sub.aCu.sub.bNi.sub.cSi.sub.dTi.sub.eZn.sub.fZr.sub.gLa.sub.hCe.sub.iW.sub.jSn.sub.kGa.sub.lFe.sub.mMO.sub.nMn.sub.oCO.sub.pO.sub.x, wherein a, b, c, d, g, h, i, j, k, l, m n, o, p and x are the molar ratios of the respective elements, wherein a, b, c, d, h, i, j, k, l, m, n, o and p are >0, e, f and g are >0 and x is such that the catalyst is electrically neutral.

Catalysts for the deoxygenation of esters of free fatty acids and triglycerides

It is provided solid, heterogeneous catalysts for the deoxygenation of esters of free fatty acids and triglycerides, and for the production of hydrocarbons that can be used as biofuels. More particularly, the catalyst comprises at least one metal oxide, the catalyst having a formula Al.sub.aCu.sub.bNi.sub.cSi.sub.dTi.sub.eZn.sub.fZr.sub.gLa.sub.hCe.sub.iW.sub.jSn.sub.kGa.sub.lFe.sub.mMO.sub.nMn.sub.oCO.sub.pO.sub.x, wherein a, b, c, d, g, h, i, j, k, l, m n, o, p and x are the molar ratios of the respective elements, wherein a, b, c, d, h, i, j, k, l, m, n, o and p are >0, e, f and g are >0 and x is such that the catalyst is electrically neutral.

Lubricant Compositions Containing Hexene-Based Oligomers
20180265799 · 2018-09-20 ·

Disclosed herein are oligomerization processes using feedstocks containing 1-hexene to produce an oligomer product, and methods for recovering a heavy 1-hexene oligomer from the oligomer product and hydrogenating the heavy 1-hexene oligomer. The resultant hydrogenated heavy 1-hexene oligomer can be blended with other PAO's to form 100 cSt and 40 cSt lubricant compositions, which have viscosity index and pour point properties that are equivalent to or better than respective 100 cSt and 40 cSt 1-decene PAO's.

Lubricant Compositions Containing Hexene-Based Oligomers
20180265799 · 2018-09-20 ·

Disclosed herein are oligomerization processes using feedstocks containing 1-hexene to produce an oligomer product, and methods for recovering a heavy 1-hexene oligomer from the oligomer product and hydrogenating the heavy 1-hexene oligomer. The resultant hydrogenated heavy 1-hexene oligomer can be blended with other PAO's to form 100 cSt and 40 cSt lubricant compositions, which have viscosity index and pour point properties that are equivalent to or better than respective 100 cSt and 40 cSt 1-decene PAO's.

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.

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.

Low carbon footprint process for regenerating sulfuric acid and recovering hydrocarbons from a spent sulfuric acid catalyst from an alkylation unit
09962687 · 2018-05-08 ·

A method for regenerating a spent sulfuric acid catalyst and recovering hydrocarbons from a spent sulfuric acid catalyst from alkylation of olefins and alkanes by using a hydrophobic supported liquid membrane is provided.

Low carbon footprint process for regenerating sulfuric acid and recovering hydrocarbons from a spent sulfuric acid catalyst from an alkylation unit
09962687 · 2018-05-08 ·

A method for regenerating a spent sulfuric acid catalyst and recovering hydrocarbons from a spent sulfuric acid catalyst from alkylation of olefins and alkanes by using a hydrophobic supported liquid membrane is provided.

REMOVAL OF SULFUR FROM NAPHTHA

A process and apparatus for reducing the sulfur content of naphtha. The process includes introducing at least a portion of a naphtha feed stream to a selective hydrodesulfurization zone under selective hydrodesulfurization conditions in the presence of a selective hydrodesulfurization catalyst to form a low sulfur stream which contains mercaptan and thiophene compounds. At least a portion of the low sulfur stream is separated into at least two streams, a mercaptan rich stream containing mercaptan and thiophene compounds and an overhead stream containing hydrogen sulfide and liquid petroleum gas. The mercaptan rich stream is treated in an adsorbent zone to remove at least a portion of the mercaptan and thiophene compounds to form a mercaptan lean stream.