Kinetics of the synergy effects in heavy oil upgrading using novel Ni-p-tert-butylcalix[4]arene as a dispersed catalyst with a supported catalyst

This study investigates the promotional effects of implementing a co-catalytic system for hydrocracking of vacuum gas oil (VGO) that includes both dispersed and supported solid catalysts. A novel nickel-based p-tert-butylcalix[4]arene (Ni-TBC[4]) was employed as a dispersed catalyst in addition to a...

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Veröffentlicht in:Fuel processing technology 2019-03, Vol.185, p.158-168
Hauptverfasser: Al-Attas, Tareq A., Zahir, Md. Hassan, Ali, Syed A., Al-Bogami, Saad A., Malaibari, Zuhair, Razzak, Shaikh A., Hossain, Mohammad M.
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container_end_page 168
container_issue
container_start_page 158
container_title Fuel processing technology
container_volume 185
creator Al-Attas, Tareq A.
Zahir, Md. Hassan
Ali, Syed A.
Al-Bogami, Saad A.
Malaibari, Zuhair
Razzak, Shaikh A.
Hossain, Mohammad M.
description This study investigates the promotional effects of implementing a co-catalytic system for hydrocracking of vacuum gas oil (VGO) that includes both dispersed and supported solid catalysts. A novel nickel-based p-tert-butylcalix[4]arene (Ni-TBC[4]) was employed as a dispersed catalyst in addition to a commercial first-stage hydrocracking supported catalyst. Slurry-phase hydrocracking was conducted isothermally under a hydrogen pressure of 8.5 MPa in a batch autoclave reactor by varying the reaction temperature (390–450 °C) and duration (0.5–1.5 h). The use of the synthesized metallocalixarene as a dispersed catalyst precursor enhanced the hydrogenation activity and noticeably reduced the coke and gas formation. The yields of coke and gases decreased upon introducing the dispersed catalyst along with the supported solid catalyst by 35.86% and 13.90%, respectively. The yield of naphtha increased from 15.27 wt% to 16.36 wt%, and that of distillate increased from 52.17 wt% to 53.57 wt% compared with the use of the supported catalyst, while the conversion of VGO was unchanged at about 83.20%. The value of the dimensionless catalytic activity parameter proved the existence of the synergy between the two catalysts since it is much higher than that acquired through the algebraically calculated yields. A five-lump discrete kinetic scheme was developed based on the experimental data governed from both the standalone supported catalyst and the mixed catalysts. The model incorporated the conversion of VGO to distillate, naphtha, and C1–C5 gaseous hydrocarbons in addition to coke deposition. The activation energy of the distillate formation was reduced from 65.39 kcal/mol to 57.32 kcal/mol by adding a Ni-TBC[4] catalyst precursor in the presence of supported catalyst. [Display omitted] •Ni-p-tert-butylcalix[4]arene (Ni-TBC[4]) is used as a dispersed catalysts in HC of VGO.•Ni-TBC[4] increased liquid yields, while decreased coke and gas formation.•A five lump discrete model represented the kinetics of the HC reaction adequately.•Activation energy of distillate was significantly decreased with Ni-TBC[4].
doi_str_mv 10.1016/j.fuproc.2018.12.003
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Hassan ; Ali, Syed A. ; Al-Bogami, Saad A. ; Malaibari, Zuhair ; Razzak, Shaikh A. ; Hossain, Mohammad M.</creator><creatorcontrib>Al-Attas, Tareq A. ; Zahir, Md. Hassan ; Ali, Syed A. ; Al-Bogami, Saad A. ; Malaibari, Zuhair ; Razzak, Shaikh A. ; Hossain, Mohammad M.</creatorcontrib><description>This study investigates the promotional effects of implementing a co-catalytic system for hydrocracking of vacuum gas oil (VGO) that includes both dispersed and supported solid catalysts. A novel nickel-based p-tert-butylcalix[4]arene (Ni-TBC[4]) was employed as a dispersed catalyst in addition to a commercial first-stage hydrocracking supported catalyst. Slurry-phase hydrocracking was conducted isothermally under a hydrogen pressure of 8.5 MPa in a batch autoclave reactor by varying the reaction temperature (390–450 °C) and duration (0.5–1.5 h). The use of the synthesized metallocalixarene as a dispersed catalyst precursor enhanced the hydrogenation activity and noticeably reduced the coke and gas formation. The yields of coke and gases decreased upon introducing the dispersed catalyst along with the supported solid catalyst by 35.86% and 13.90%, respectively. The yield of naphtha increased from 15.27 wt% to 16.36 wt%, and that of distillate increased from 52.17 wt% to 53.57 wt% compared with the use of the supported catalyst, while the conversion of VGO was unchanged at about 83.20%. The value of the dimensionless catalytic activity parameter proved the existence of the synergy between the two catalysts since it is much higher than that acquired through the algebraically calculated yields. A five-lump discrete kinetic scheme was developed based on the experimental data governed from both the standalone supported catalyst and the mixed catalysts. The model incorporated the conversion of VGO to distillate, naphtha, and C1–C5 gaseous hydrocarbons in addition to coke deposition. The activation energy of the distillate formation was reduced from 65.39 kcal/mol to 57.32 kcal/mol by adding a Ni-TBC[4] catalyst precursor in the presence of supported catalyst. [Display omitted] •Ni-p-tert-butylcalix[4]arene (Ni-TBC[4]) is used as a dispersed catalysts in HC of VGO.•Ni-TBC[4] increased liquid yields, while decreased coke and gas formation.•A five lump discrete model represented the kinetics of the HC reaction adequately.•Activation energy of distillate was significantly decreased with Ni-TBC[4].</description><identifier>ISSN: 0378-3820</identifier><identifier>EISSN: 1873-7188</identifier><identifier>DOI: 10.1016/j.fuproc.2018.12.003</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>activation energy ; aromatic hydrocarbons ; autoclaves ; Autoclaving ; Catalysis ; Catalysts ; Catalytic activity ; Chemical synthesis ; Coke oven gas ; Conversion ; Discrete lumped kinetics ; Dispersed catalysts ; Dispersion ; Distillates ; fuel oils ; Gas formation ; Gas oil ; gases ; Heavy oil upgrading ; Hydrocracking ; hydrogen ; Hydrogen storage ; hydrogenation ; Metallocalixarenes ; Naphtha ; Nickel ; p-tert-Butyl-calix[n]arene ; Precursors ; Reaction kinetics ; Slurries ; Synergy ; temperature ; VGO</subject><ispartof>Fuel processing technology, 2019-03, Vol.185, p.158-168</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. 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Hassan</creatorcontrib><creatorcontrib>Ali, Syed A.</creatorcontrib><creatorcontrib>Al-Bogami, Saad A.</creatorcontrib><creatorcontrib>Malaibari, Zuhair</creatorcontrib><creatorcontrib>Razzak, Shaikh A.</creatorcontrib><creatorcontrib>Hossain, Mohammad M.</creatorcontrib><title>Kinetics of the synergy effects in heavy oil upgrading using novel Ni-p-tert-butylcalix[4]arene as a dispersed catalyst with a supported catalyst</title><title>Fuel processing technology</title><description>This study investigates the promotional effects of implementing a co-catalytic system for hydrocracking of vacuum gas oil (VGO) that includes both dispersed and supported solid catalysts. A novel nickel-based p-tert-butylcalix[4]arene (Ni-TBC[4]) was employed as a dispersed catalyst in addition to a commercial first-stage hydrocracking supported catalyst. Slurry-phase hydrocracking was conducted isothermally under a hydrogen pressure of 8.5 MPa in a batch autoclave reactor by varying the reaction temperature (390–450 °C) and duration (0.5–1.5 h). The use of the synthesized metallocalixarene as a dispersed catalyst precursor enhanced the hydrogenation activity and noticeably reduced the coke and gas formation. The yields of coke and gases decreased upon introducing the dispersed catalyst along with the supported solid catalyst by 35.86% and 13.90%, respectively. The yield of naphtha increased from 15.27 wt% to 16.36 wt%, and that of distillate increased from 52.17 wt% to 53.57 wt% compared with the use of the supported catalyst, while the conversion of VGO was unchanged at about 83.20%. The value of the dimensionless catalytic activity parameter proved the existence of the synergy between the two catalysts since it is much higher than that acquired through the algebraically calculated yields. A five-lump discrete kinetic scheme was developed based on the experimental data governed from both the standalone supported catalyst and the mixed catalysts. The model incorporated the conversion of VGO to distillate, naphtha, and C1–C5 gaseous hydrocarbons in addition to coke deposition. The activation energy of the distillate formation was reduced from 65.39 kcal/mol to 57.32 kcal/mol by adding a Ni-TBC[4] catalyst precursor in the presence of supported catalyst. [Display omitted] •Ni-p-tert-butylcalix[4]arene (Ni-TBC[4]) is used as a dispersed catalysts in HC of VGO.•Ni-TBC[4] increased liquid yields, while decreased coke and gas formation.•A five lump discrete model represented the kinetics of the HC reaction adequately.•Activation energy of distillate was significantly decreased with Ni-TBC[4].</description><subject>activation energy</subject><subject>aromatic hydrocarbons</subject><subject>autoclaves</subject><subject>Autoclaving</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemical synthesis</subject><subject>Coke oven gas</subject><subject>Conversion</subject><subject>Discrete lumped kinetics</subject><subject>Dispersed catalysts</subject><subject>Dispersion</subject><subject>Distillates</subject><subject>fuel oils</subject><subject>Gas formation</subject><subject>Gas oil</subject><subject>gases</subject><subject>Heavy oil upgrading</subject><subject>Hydrocracking</subject><subject>hydrogen</subject><subject>Hydrogen storage</subject><subject>hydrogenation</subject><subject>Metallocalixarenes</subject><subject>Naphtha</subject><subject>Nickel</subject><subject>p-tert-Butyl-calix[n]arene</subject><subject>Precursors</subject><subject>Reaction kinetics</subject><subject>Slurries</subject><subject>Synergy</subject><subject>temperature</subject><subject>VGO</subject><issn>0378-3820</issn><issn>1873-7188</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kU1v1DAQhiMEEkvhH3CwxIVLUo8_EueChCq-1Kpc6Akhy2uPd71K42A7W_Iz-o_JajkgDlxmDvO-r2bmqarXQBug0F4eGj9PKdqGUVANsIZS_qTagOp43YFST6sN5Z2quWL0efUi5wOlVMq-21SP12HEEmwm0ZOyR5KXEdNuIeg92pJJGMkezXEhMQxknnbJuDDuyJxPdYxHHMhtqKe6YCr1di7LYM0Qfn0XP0zCEYnJxBAX8oQpoyPWFDMsuZCHUPbrJM_TFFP5a_KyeubNkPHVn35R3X388O3qc33z9dOXq_c3tRVUlNpzL7jdGi9USyVw1kop3JZC33tmrGCoRK8AnATLXMtA9tRSlMxb6kQn-UX19py7fu7njLno-5AtDoMZMc5ZM8aAMsmBr9I3_0gPcU7jup1m0ClgooV-VYmzyqaYc0KvpxTuTVo0UH3ipA_6zEmfOGlgeuW02t6dbbgeewyYdLYBR4supJWAdjH8P-A30rWfRw</recordid><startdate>20190301</startdate><enddate>20190301</enddate><creator>Al-Attas, Tareq A.</creator><creator>Zahir, Md. 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Hassan</creatorcontrib><creatorcontrib>Ali, Syed A.</creatorcontrib><creatorcontrib>Al-Bogami, Saad A.</creatorcontrib><creatorcontrib>Malaibari, Zuhair</creatorcontrib><creatorcontrib>Razzak, Shaikh A.</creatorcontrib><creatorcontrib>Hossain, Mohammad M.</creatorcontrib><collection>CrossRef</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Fuel processing technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Attas, Tareq A.</au><au>Zahir, Md. Hassan</au><au>Ali, Syed A.</au><au>Al-Bogami, Saad A.</au><au>Malaibari, Zuhair</au><au>Razzak, Shaikh A.</au><au>Hossain, Mohammad M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of the synergy effects in heavy oil upgrading using novel Ni-p-tert-butylcalix[4]arene as a dispersed catalyst with a supported catalyst</atitle><jtitle>Fuel processing technology</jtitle><date>2019-03-01</date><risdate>2019</risdate><volume>185</volume><spage>158</spage><epage>168</epage><pages>158-168</pages><issn>0378-3820</issn><eissn>1873-7188</eissn><abstract>This study investigates the promotional effects of implementing a co-catalytic system for hydrocracking of vacuum gas oil (VGO) that includes both dispersed and supported solid catalysts. A novel nickel-based p-tert-butylcalix[4]arene (Ni-TBC[4]) was employed as a dispersed catalyst in addition to a commercial first-stage hydrocracking supported catalyst. Slurry-phase hydrocracking was conducted isothermally under a hydrogen pressure of 8.5 MPa in a batch autoclave reactor by varying the reaction temperature (390–450 °C) and duration (0.5–1.5 h). The use of the synthesized metallocalixarene as a dispersed catalyst precursor enhanced the hydrogenation activity and noticeably reduced the coke and gas formation. The yields of coke and gases decreased upon introducing the dispersed catalyst along with the supported solid catalyst by 35.86% and 13.90%, respectively. The yield of naphtha increased from 15.27 wt% to 16.36 wt%, and that of distillate increased from 52.17 wt% to 53.57 wt% compared with the use of the supported catalyst, while the conversion of VGO was unchanged at about 83.20%. The value of the dimensionless catalytic activity parameter proved the existence of the synergy between the two catalysts since it is much higher than that acquired through the algebraically calculated yields. A five-lump discrete kinetic scheme was developed based on the experimental data governed from both the standalone supported catalyst and the mixed catalysts. The model incorporated the conversion of VGO to distillate, naphtha, and C1–C5 gaseous hydrocarbons in addition to coke deposition. The activation energy of the distillate formation was reduced from 65.39 kcal/mol to 57.32 kcal/mol by adding a Ni-TBC[4] catalyst precursor in the presence of supported catalyst. [Display omitted] •Ni-p-tert-butylcalix[4]arene (Ni-TBC[4]) is used as a dispersed catalysts in HC of VGO.•Ni-TBC[4] increased liquid yields, while decreased coke and gas formation.•A five lump discrete model represented the kinetics of the HC reaction adequately.•Activation energy of distillate was significantly decreased with Ni-TBC[4].</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.fuproc.2018.12.003</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-3590-2912</orcidid></addata></record>
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identifier ISSN: 0378-3820
ispartof Fuel processing technology, 2019-03, Vol.185, p.158-168
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1873-7188
language eng
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source Elsevier ScienceDirect Journals Complete
subjects activation energy
aromatic hydrocarbons
autoclaves
Autoclaving
Catalysis
Catalysts
Catalytic activity
Chemical synthesis
Coke oven gas
Conversion
Discrete lumped kinetics
Dispersed catalysts
Dispersion
Distillates
fuel oils
Gas formation
Gas oil
gases
Heavy oil upgrading
Hydrocracking
hydrogen
Hydrogen storage
hydrogenation
Metallocalixarenes
Naphtha
Nickel
p-tert-Butyl-calix[n]arene
Precursors
Reaction kinetics
Slurries
Synergy
temperature
VGO
title Kinetics of the synergy effects in heavy oil upgrading using novel Ni-p-tert-butylcalix[4]arene as a dispersed catalyst with a supported catalyst
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