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One-pot Selective Conversion of Biomass-derived Furfural into Cyclopentanone/Cyclopentanol over TiO2 Supported Bimetallic Ni-M (M = Co, Fe) Catalysts

Bulletin of Chemical Reaction Engineering & Catalysis · Vol. ume (2020) · hlm. 231–241

DOI
10.9767/bcrec.15.1.6307.231-241
ISSN
1978-2993
Terbit
2020-04-01
Penerbit
Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-sa/4.0

Abstrak

One-pot selective conversion of biomass-derived furfural (FFald) into cyclopentanone (CPO) or cyclopentanol (CPL) using bimetallic nickel-based supported on TiO2 (denoted as Ni-M(3.0)/TiO2; M = Co and Fe; 3.0 is Ni/M molar ratio) have been investigated. Catalysts were synthesized via a hydrothermal method at 150 °C for 24 h, followed by H2 reduction at 450 °C for 1.5 h. X-ray Diffraction (XRD) analysis showed that the formation of Ni-Co alloy phase at 2θ = 44.2° for Ni-Co(3.0)/TiO2 and Ni-Fe alloy at 2θ = 44.1° for Ni-Fe(3.0)/TiO2. The amount of acid sites was measured by using ammonia-temperature programmed desorption (NH3-TPD). Ni-Co(3.0)/TiO2 has three NH3 desorption peaks at 180 °C, 353 °C, and 569 °C with acid site amounts of 1.30 µmol.g-1, 1.0 µmol.g-1, and 2.0 µmol.g-1, respectively. On the other hand, Ni-Fe(3.0)/TiO2 consisted of NH3 desorption peaks at 214 °C and 626 °C with acid site amounts of 3.3 µmol.g-1and 2.0 µmol.g-1, respectively. Both Ni-Co(3.0)/TiO2 and Ni-Fe(3.0)/TiO2 catalysts were found to be active for the selective hydrogenation of FFald to furfuryl alcohol (FFalc) at low temperature of 110 °C, H2 3.0 MPa, 3 h with FFalc selectivity of 81.1% and 82.9%, respectively. High yields of CPO (27.2%) and CPL (41.0%) were achieved upon Ni-Fe(3.0)/TiO2 when the reaction temperature was increased to 170 °C, 3.0 MPa of H2, and a reaction time of 6 h. The yield of CPO+CPL on the reused catalyst decreased slightly after the second reaction run, but the activity was maintained for at least three consecutive runs. Copyright © 2020 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

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  • Lambung Mangkurat University
  • National Research and Innovation Agency
  • Chiba University
  • Sultan Ageng Tirtayasa University
  • Tanjungpura University
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Rekan penulisOrganisasiArtikel bersama
Atina Sabila AzzahraLambung Mangkurat University6
Sadang HusainLambung Mangkurat University6
Agung NugrohoLambung Mangkurat University4
Shogo ShimazuChiba University3
Pathur Razi AnsyahLambung Mangkurat University2
Edi MikriantoLambung Mangkurat University2
Thea Seventina Desiani BodoiLambung Mangkurat University2
Gagus Ketut SunnardiantoNational Research and Innovation Agency2
Muhammad Iqbal PratamaLambung Mangkurat University2
Abdullah AbdullahLambung Mangkurat University2
Susi SusiLambung Mangkurat University2
Sutomo SutomoLambung Mangkurat University2
Elisa HayatiLambung Mangkurat University2
Kamilia MustikasariLambung Mangkurat University2
Sutomo SutomoLambung Mangkurat University2
Syahrul KhairiTanjungpura University2
Kurnia PutriLambung Mangkurat University1
Annisa AnnisaLambung Mangkurat University1
Arif RidhoniAfiliasi tidak diketahui1
Ikhsan MustariAfiliasi tidak diketahui1
Anggita NurfitrianiAfiliasi tidak diketahui1
Rahmat Eko SanjayaLambung Mangkurat University1
Eka SuarsoLambung Mangkurat University1
Iryanti Fatyasari NataLambung Mangkurat University1
Kiky Corneliasari SembiringNational Research and Innovation Agency1
Heny Puspita DewiLambung Mangkurat University1
Jayanudin JayanudinSultan Ageng Tirtayasa University1
Indri Badri AdilinaAfiliasi tidak diketahui1
Utami IrawatiLambung Mangkurat University1
Shauqi Aulia RifwandaLambung Mangkurat University1
Ferensa OemryNational Research and Innovation Agency1
Takayoshi HaraChiba University1
Dewi UmaningrumLambung Mangkurat University1
Uripto Trisno SantosoLambung Mangkurat University1
Radna NurmasariLambung Mangkurat University1
Hapsari Tyas PraditaLambung Mangkurat University1

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Sumber metadata: OAI-PMH (metadata jurnal) https://journal.bcrec.id/index.php/bcrec/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en-US">One-pot Selective Conversion of Biomass-derived Furfural into Cyclopentanone/Cyclopentanol over TiO2 Supported Bimetallic Ni-M (M = Co, Fe) Catalysts</dc:title>
	<dc:creator>Astuti, Maria Dewi</dc:creator>
	<dc:creator>Kristina, Ditya</dc:creator>
	<dc:creator>Rodiansono, Rodiansono</dc:creator>
	<dc:creator>Mujiyanti, Dwi Rasy</dc:creator>
	<dc:subject xml:lang="en-US">Bimetallic Ni-M (M=Co and Fe); Furfural; Furfuryl alcohol; Cyclopentanone; Cyclopentanol</dc:subject>
	<dc:description xml:lang="en-US">One-pot selective conversion of biomass-derived furfural (FFald) into cyclopentanone (CPO) or cyclopentanol (CPL) using bimetallic nickel-based supported on TiO2 (denoted as Ni-M(3.0)/TiO2; M = Co and Fe; 3.0 is Ni/M molar ratio) have been investigated. Catalysts were synthesized via a hydrothermal method at 150 °C for 24 h, followed by H2 reduction at 450 °C for 1.5 h. X-ray Diffraction (XRD) analysis  showed that the formation of Ni-Co alloy phase at 2θ = 44.2° for Ni-Co(3.0)/TiO2 and Ni-Fe alloy at 2θ = 44.1° for Ni-Fe(3.0)/TiO2. The amount of acid sites was measured by using ammonia-temperature programmed desorption (NH3-TPD). Ni-Co(3.0)/TiO2 has three NH3 desorption peaks at 180 °C, 353 °C, and 569 °C with acid site amounts of 1.30 µmol.g-1, 1.0 µmol.g-1, and 2.0 µmol.g-1,        respectively. On the other hand, Ni-Fe(3.0)/TiO2 consisted of NH3 desorption peaks at 214 °C and 626 °C with acid site amounts of 3.3 µmol.g-1and 2.0 µmol.g-1, respectively. Both Ni-Co(3.0)/TiO2 and Ni-Fe(3.0)/TiO2 catalysts were found to be active for the selective hydrogenation of FFald to furfuryl alcohol (FFalc) at low temperature of 110 °C, H2 3.0 MPa, 3 h with FFalc selectivity of 81.1% and 82.9%, respectively. High yields of CPO (27.2%) and CPL (41.0%) were achieved upon Ni-Fe(3.0)/TiO2 when the reaction temperature was increased to 170 °C, 3.0 MPa of H2, and a reaction time of 6 h. The yield of CPO+CPL on the reused catalyst decreased slightly after the second reaction run, but the activity was maintained for at least three consecutive runs. Copyright © 2020 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). </dc:description>
	<dc:publisher xml:lang="en-US">Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)</dc:publisher>
	<dc:contributor xml:lang="en-US">Penelitian Berbasis Kompetensi (PBK) FY 2017-2018 under grant number of DIPA-042.06-1.401516/2018 and DIPA-042.06-1.401516/2019, Ministry of Research, Technology, and Higher Education, Indonesian Government</dc:contributor>
	<dc:date>2020-04-01</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US"></dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.bcrec.id/index.php/bcrec/article/view/6307</dc:identifier>
	<dc:identifier>10.9767/bcrec.15.1.6307.231-241</dc:identifier>
	<dc:source xml:lang="en-US">Bulletin of Chemical Reaction Engineering &amp; Catalysis; 2020: BCREC Volume 15 Issue 1 Year 2020 (April 2020); 231-241</dc:source>
	<dc:source>1978-2993</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.bcrec.id/index.php/bcrec/article/view/6307/3652</dc:relation>
	<dc:relation>https://journal.bcrec.id/index.php/bcrec/article/downloadSuppFile/6307/1446</dc:relation>
	<dc:relation>https://journal.bcrec.id/index.php/bcrec/article/downloadSuppFile/6307/1448</dc:relation>
	<dc:relation>https://journal.bcrec.id/index.php/bcrec/article/downloadSuppFile/6307/1451</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2020 by Authors, Published by BCREC Group</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-sa/4.0</dc:rights>
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