US2012316093A1PendingUtilityA1

Conversion of fatty acids to base oils and transportation fuels

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Assignee: ZHAN BI-ZENGPriority: Jun 10, 2011Filed: Jun 10, 2011Published: Dec 13, 2012
Est. expiryJun 10, 2031(~4.9 yrs left)· nominal 20-yr term from priority
C10G 3/42C10G 2300/1011C10G 2400/10C10N 2020/065C10N 2020/011C10L 1/08C10G 45/64Y02P30/20C10M 2203/003C10G 2300/302C10N 2030/02C10M 2203/1025C10G 65/043C10N 2070/00C10G 2400/04C10G 45/58Y02P20/582C10M 105/04C10L 10/12C10G 45/62Y02E50/10
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Claims

Abstract

The present invention is directed to methods for processing fatty acids to provide for base oil and transportation fuels, wherein decarboxylation-coupling dimerization of fatty acids provides dimer ketones from which the base oils and transportation fuels may be produced.

Claims

exact text as granted — not AI-modified
1 . A method comprising:
 a) contacting a fatty acid feed with a decarboxylation-coupling dimerization catalyst in a decarboxylation-coupling dimerization zone under decarboxylation-coupling dimerization conditions to yield a dimer ketone;   b) hydrocracking the dimer ketone with a hydrocracking catalyst in a hydrocracking zone under hydrocracking conditions to yield a mixture of paraffins comprising a heavy waxy oil component and a diesel fuel component; and   c) distilling the mixture to yield a heavy waxy oil and a diesel fuel.   
     
     
         2 . The method of  claim 1 , wherein the fatty acid feed is derived from biomass. 
     
     
         3 . The method of  claim 1 , wherein the fatty acid feed comprises at least 75 wt. % saturated fatty acids. 
     
     
         4 . The method of  claim 3 , wherein the saturated fatty acids are selected from the group consisting of caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, palm kernel oil acid, coconut oil acid, and combinations thereof. 
     
     
         5 . The method of  claim 1 , wherein the decarboxylation-coupling dimerization catalyst is selected from the group consisting of alumina, silica, silica-alumina, titania, zirconia, and combinations thereof. 
     
     
         6 . The method of  claim 1 , wherein the decarboxylation-coupling dimerization catalyst is a supported metal carbonate or hydroxide. 
     
     
         7 . The method of  claim 1 , wherein the diesel fuel is a biofuel. 
     
     
         8 . The method of  claim 1 , wherein the diesel fuel has a cetane index of at least 65. 
     
     
         9 . The method of  claim 1 , further comprising hydroisomerization dewaxing the heavy waxy oil with a hydroisomerization dewaxing catalyst in a catalytic hydroisomerization dewaxing zone under hydroisomerization dewaxing conditions to yield a lubricating base oil. 
     
     
         10 . The method of  claim 9 , wherein the hydroisomerization catalyst comprises a shape selective intermediate pore size molecular sieve, a noble metal hydrogenation component, and at least a refractory oxide support. 
     
     
         11 . The method of  claim 10 , wherein the molecular sieve is selected from the group consisting of SAPO-11, SAPO-31, SAPO-41, SM-3, SM-7, ZSM-22, ZSM-23, ZSM-35, ZSM-48, ZSM-57, SSZ-32, ferrierite, and combinations thereof. 
     
     
         12 . The method of  claim 9 , wherein the base oil has a viscosity index of at least 140. 
     
     
         13 . The method of  claim 9 , wherein the base oil has a viscosity index of at least 170. 
     
     
         14 . The method of  claim 9 , wherein the base oil is a Group III base oil. 
     
     
         15 . The method of  claim 9 , further comprising a step of hydrofinishing the base oil. 
     
     
         16 . A method comprising:
 a) contacting a fatty acid feed with a decarboxylation-coupling dimerization catalyst in a decarboxylation-coupling dimerization zone under decarboxylation-coupling dimerization conditions to yield a dimer ketone; and   b) hydroisomerization dewaxing the dimer ketone with a hydroisomerization dewaxing catalyst in a catalytic hydroisomerization zone under hydroisomerization dewaxing conditions to yield a lubricating base oil.   
     
     
         17 . The method of  claim 16 , wherein the base oil has a viscosity index of at least 140. 
     
     
         18 . The method of  claim 16 , wherein the base oil has a viscosity index of at least 170. 
     
     
         19 . The method of  claim 16 , wherein the base oil is a Group III base oil. 
     
     
         20 . The method of  claim 16 , further comprising a step of hydrofinishing the base oil.

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