Rational design of efficient polar heterogeneous catalysts for catalytic oxidative-adsorptive desulfurization in fuel oil

The rational design of efficient polar heterogeneous catalysts for oxidation adsorption desulfurization (OADS) is still a challenge. Herein, we fabricated a novel polar fingerprint-like heterogeneous catalyst (HPW-NH2-CPRNSs) by immobilizing phosphotungstic acid on amino grafted phenolic resin nanos...

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Published inApplied catalysis. A, General Vol. 632; p. 118498
Main Authors Zhang, Yuqi, Yang, Wanliang, Yang, Xue, Tang, Manqi, Yang, Kuo, Li, Feng, Zhou, Wending, Xu, Meisong
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 25.02.2022
Elsevier Science SA
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Abstract The rational design of efficient polar heterogeneous catalysts for oxidation adsorption desulfurization (OADS) is still a challenge. Herein, we fabricated a novel polar fingerprint-like heterogeneous catalyst (HPW-NH2-CPRNSs) by immobilizing phosphotungstic acid on amino grafted phenolic resin nanospheres prepared through gradient temperature hydrothermal method, which exhibits highly effective oxidative-adsorptive desulfurization (OADS) performance. The fingerprint-like nanospheres catalysts were formed when the F127 exposed on the surface of PRNSs was dissolved during the refluxing. Moreover, the polarity of the HPW-NH2-CPRNSs catalysts can be well adjusted by controlling the amount of amino grafting and calcination temperature, which plays an important role in OADS. The removal rate of DBT on optimal polar catalyst reached the highest 98.9% in 90 min. It is the first time that this work involving the phenolic resin polymers have been used as the carrier of desulfurization catalyst and the polarity of the catalyst has been artificially controlled for OADS. A novel phenolic resin-based catalyst (HPW-NH2-CPRNSs) with controllable polarity and fingerprint-like appearance was successfully synthesized as both catalyst and adsorbent for highly effective and stable oxidative-adsorptive desulfurization. [Display omitted] •Fingerprint-like HPW-NH2-CPRNSs was successfully prepared for OADS in fuel oil.•The polarity of PR-based catalysts was adjusted by tuning the amount of -NH2 and temperature.•The polarity of PR-based catalyst plays an important role in OADS.•The removal rate of DBT on optimal polar catalyst reached the highest 98.9% in 90 min
AbstractList The rational design of efficient polar heterogeneous catalysts for oxidation adsorption desulfurization (OADS) is still a challenge. Herein, we fabricated a novel polar fingerprint-like heterogeneous catalyst (HPW-NH2-CPRNSs) by immobilizing phosphotungstic acid on amino grafted phenolic resin nanospheres prepared through gradient temperature hydrothermal method, which exhibits highly effective oxidative-adsorptive desulfurization (OADS) performance. The fingerprint-like nanospheres catalysts were formed when the F127 exposed on the surface of PRNSs was dissolved during the refluxing. Moreover, the polarity of the HPW-NH2-CPRNSs catalysts can be well adjusted by controlling the amount of amino grafting and calcination temperature, which plays an important role in OADS. The removal rate of DBT on optimal polar catalyst reached the highest 98.9% in 90 min. It is the first time that this work involving the phenolic resin polymers have been used as the carrier of desulfurization catalyst and the polarity of the catalyst has been artificially controlled for OADS.
The rational design of efficient polar heterogeneous catalysts for oxidation adsorption desulfurization (OADS) is still a challenge. Herein, we fabricated a novel polar fingerprint-like heterogeneous catalyst (HPW-NH2-CPRNSs) by immobilizing phosphotungstic acid on amino grafted phenolic resin nanospheres prepared through gradient temperature hydrothermal method, which exhibits highly effective oxidative-adsorptive desulfurization (OADS) performance. The fingerprint-like nanospheres catalysts were formed when the F127 exposed on the surface of PRNSs was dissolved during the refluxing. Moreover, the polarity of the HPW-NH2-CPRNSs catalysts can be well adjusted by controlling the amount of amino grafting and calcination temperature, which plays an important role in OADS. The removal rate of DBT on optimal polar catalyst reached the highest 98.9% in 90 min. It is the first time that this work involving the phenolic resin polymers have been used as the carrier of desulfurization catalyst and the polarity of the catalyst has been artificially controlled for OADS. A novel phenolic resin-based catalyst (HPW-NH2-CPRNSs) with controllable polarity and fingerprint-like appearance was successfully synthesized as both catalyst and adsorbent for highly effective and stable oxidative-adsorptive desulfurization. [Display omitted] •Fingerprint-like HPW-NH2-CPRNSs was successfully prepared for OADS in fuel oil.•The polarity of PR-based catalysts was adjusted by tuning the amount of -NH2 and temperature.•The polarity of PR-based catalyst plays an important role in OADS.•The removal rate of DBT on optimal polar catalyst reached the highest 98.9% in 90 min
ArticleNumber 118498
Author Zhang, Yuqi
Zhou, Wending
Yang, Kuo
Li, Feng
Xu, Meisong
Yang, Xue
Yang, Wanliang
Tang, Manqi
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CitedBy_id crossref_primary_10_1016_j_jece_2022_107298
crossref_primary_10_1177_18479804221106321
crossref_primary_10_1016_j_fuel_2022_125370
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Keywords Phosphotungstic acid immobilized
Fingerprint-like composites
Oxidative-adsorptive desulfurization
Polar heterogeneous catalysts
HPW-NH2-CPRNSs
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Snippet The rational design of efficient polar heterogeneous catalysts for oxidation adsorption desulfurization (OADS) is still a challenge. Herein, we fabricated a...
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StartPage 118498
SubjectTerms Adsorptivity
Catalysts
Desulfurizing
Fingerprint-like composites
Fingerprints
Fuel oils
HPW-NH2-CPRNSs
Nanospheres
Oxidation
Oxidative-adsorptive desulfurization
Phenolic resins
Phosphotungstic acid immobilized
Polar heterogeneous catalysts
Refluxing
Title Rational design of efficient polar heterogeneous catalysts for catalytic oxidative-adsorptive desulfurization in fuel oil
URI https://dx.doi.org/10.1016/j.apcata.2022.118498
https://www.proquest.com/docview/2639708969
Volume 632
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