US2009023968A1PendingUtilityA1

Catalyst and process for producing light aromatic hydrocarbons and light alkanes from hydrocarbonaceous feedstock

Assignee: CHINA PETROLEUM & CHEMICALPriority: Jul 18, 2007Filed: Jul 18, 2008Published: Jan 22, 2009
Est. expiryJul 18, 2027(~1 yrs left)· nominal 20-yr term from priority
B01J 29/22B01J 37/10B01J 29/74B01J 29/44B01J 29/126B01J 37/0018B01J 29/80B01J 29/068B01J 29/7415B01J 29/405B01J 37/0009B01J 21/12B01J 23/42B01J 23/44
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Claims

Abstract

The present invention provides a catalyst comprising metallic Pt and/or Pd supported on a binder-free zeolite for producing light aromatic hydrocarbons and light alkanes from hydrocarbonaceous feedstock, wherein the amount of metallic Pt and/or Pd is of 0.01-0.8 wt %, preferably 0.01-0.5 wt % on the basis of the total weight of the catalyst, and the binder-free zeolite is selected from the group consisting of mordenite, beta zeolite, Y zeolite, ZSM-5, ZSM-11 and composite or cocrystal zeolite thereof. The present invention also provides a process for producing light aromatic hydrocarbons and light alkanes from hydrocarbonaceous feedstock using said catalyst.

Claims

exact text as granted — not AI-modified
1 . A catalyst comprising metallic Pt and/or Pd supported on a binder-free zeolite for producing light aromatic hydrocarbons and light alkanes from hydrocarbonaceous feedstock, wherein the amount of metallic Pt and/or Pd is of 0.01-0.8 wt %, preferably 0.01-0.5 wt % on the basis of the total weight of the catalyst, and the binder-free zeolite is selected from the group consisting of mordenite, beta zeolite, Y zeolite, ZSM-5, ZSM-11 and composite or cocrystal zeolite thereof. 
   
   
       2 . The catalyst according to  claim 1 , wherein the binder-free zeolite is ZSM-5, mordenite, beta zeolite, ZSM-5/USY composite zeolite, ZSM-5/beta composite zeolite, or ZSM-5/ZSM-11 cocrystal zeolite. 
   
   
       3 . The catalyst according to  claim 1 , further comprising a promoter selected from the group consisting of Cu, Zn, Sn, Pb, Fe and mixture thereof in amount of less than 1 wt %, preferably less than 0.6 wt % on the basis of the total weight of the catalyst. 
   
   
       4 . The catalyst according to  claim 3 , wherein the promoter is selected from the group consisting of Zn, Sn, Pb and mixture thereof. 
   
   
       5 . The catalyst according to  claim 4 , wherein the promoter is Zn. 
   
   
       6 . The catalyst according to  claim 1 , wherein the binder-free zeolite has a molar ratio SiO 2 /Al 2 O 3  in range of 10-200, preferably 20-100. 
   
   
       7 . The catalyst according to  claim 2 , further comprising a promoter selected from the group consisting of Cu, Zn, Sn, Pb, Fe and mixture thereof in amount of less than 1 wt %, preferably less than 0.6 wt % on the basis of the total weight of the catalyst. 
   
   
       8 . The catalyst according to  claim 7 , wherein the promoter is Zn. 
   
   
       9 . The catalyst according to  claim 8 , wherein the binder-free zeolite has a molar ratio SiO 2 /Al 2 O 3  in range of 10-200, preferably 20-100. 
   
   
       10 . A process for producing light aromatic hydrocarbons and light alkanes from hydrocarbonaceous feedstock, comprising the following steps:
 (a) introducing hydrogen and a hydrocarbonaceous feedstock having boiling point in range of 30-250° C. into at least one reaction zone;   (b) converting the hydrocarbonaceous feedstock to an effluent enriched in light aromatic hydrocarbons of benzene, toluene and xylene and light alkanes in the reaction zone in the presence of the catalyst according to any one of  claims 1  to  9 , wherein of the hydrocarbonaceous feedstock the heavy aromatic hydrocarbons are subjected to hydrodealkylation and/or transalkylation with light aromatic hydrocarbon, the light aromatic hydrocarbons are subjected to isomerization and the non-aromatic hydrocarbons are subjected to hydrocracking reaction; and   (c) recovering the light aromatic hydrocarbons and the light alkanes respectively by passing the effluent through gas-liquid separation and distillation sequentially, and the separated heavy fraction is recycled to the reaction zone for further reaction.   
   
   
       11 . The process according to  claim 10 , wherein in step (a) the hydrocarbonaceous feedstock is introduced into the reaction zone at a weight hour space velocity of 0.5-10 hr −1 , preferably 1-4 hr −1 , and the molar ratio of hydrogen to the hydrocarbonaceous feedstock is of 0.5:1-10:1, preferably 2:1-8:1. 
   
   
       12 . The process according to  claim 10 , wherein in step (b) the reaction temperature is of 250-600° C., preferably 300-500° C., and the reaction pressure is of 0.5-5.0 MPa, preferably 2.0-4.0 MPa. 
   
   
       13 . The process according to  claim 10 , wherein the hydrocarbonaceous feedstock is selected from the group consisting of reformate, pyrolysis gasoline, naphtha and mixture thereof. 
   
   
       14 . The process according to  claim 10 , wherein in step (c) passing the effluent through a gas-liquid separator to obtain first overhead stream comprising hydrogen, methane, ethane and LPG and first bottom stream comprising aromatic hydrocarbons as well as residual hydrogen and non-aromatic hydrocarbons, recovering LPG from the first overhead stream; and passing the first bottom stream through a distillation column to obtain second overhead stream comprising residual hydrogen and non-aromatic hydrocarbons and second bottom stream comprising aromatic hydrocarbons, further recovering LPG from the second overhead stream, and recovering aromatic hydrocarbons from the second bottom stream. 
   
   
       15 . The process according to  claim 11 , wherein in step (b) the reaction temperature is of 250-600° C., preferably 300-500° C., and the reaction pressure is of 0.5-5.0 MPa, preferably 2.0-4.0 MPa 
   
   
       16 . The process according to  claim 11 , wherein the hydrocarbonaceous feedstock is selected from the group consisting of reformate, pyrolysis gasoline, naphtha and mixture thereof. 
   
   
       17 . The process according to  claim 11 , wherein in step (c) passing the effluent through a gas-liquid separator to obtain first overhead stream comprising hydrogen, methane, ethane and LPG and first bottom stream comprising aromatic hydrocarbons as well as residual hydrogen and non-aromatic hydrocarbons, recovering LPG from the first overhead stream; and passing the first bottom stream through a distillation column to obtain second overhead stream comprising residual hydrogen and non-aromatic hydrocarbons and second bottom stream comprising aromatic hydrocarbons, further recovering LPG from the second overhead stream, and recovering aromatic hydrocarbons from the second bottom stream.

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