Highly Effective Non-Noble MnO 2 Catalysts for 5-Hydroxymethylfurfural Oxidation to 2,5-Furandicarboxylic Acid
Noble metal-free catalyst or catalytic oxidation of 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid are proposed in this study as a proposal to solve one of the great disadvantages of this reaction of using preferably noble metal-based catalysts. The catalytic activity of six MnO crystal str...
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Published in | ChemSusChem Vol. 17; no. 14; p. e202400115 |
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Format | Journal Article |
Language | English |
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22.07.2024
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Abstract | Noble metal-free catalyst or catalytic oxidation of 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid are proposed in this study as a proposal to solve one of the great disadvantages of this reaction of using preferably noble metal-based catalysts. The catalytic activity of six MnO
crystal structures is studied as alternative. The obtained results showed a strong connection between catalytic activity the type of MnO
structure organization and redox behavior. Among all tested catalysts, ϵ-MnO
showed the best performance with an excellent yield of 74 % of 2,5-furandicarboxylic acid at full -hydroxymethylfurfural conversion. |
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AbstractList | Noble metal-free catalyst or catalytic oxidation of 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid are proposed in this study as a proposal to solve one of the great disadvantages of this reaction of using preferably noble metal-based catalysts. The catalytic activity of six MnO
crystal structures is studied as alternative. The obtained results showed a strong connection between catalytic activity the type of MnO
structure organization and redox behavior. Among all tested catalysts, ϵ-MnO
showed the best performance with an excellent yield of 74 % of 2,5-furandicarboxylic acid at full -hydroxymethylfurfural conversion. Abstract Noble metal‐free catalyst or catalytic oxidation of 5‐hydroxymethylfurfural into 2,5‐furandicarboxylic acid are proposed in this study as a proposal to solve one of the great disadvantages of this reaction of using preferably noble metal‐based catalysts. The catalytic activity of six MnO 2 crystal structures is studied as alternative. The obtained results showed a strong connection between catalytic activity the type of MnO 2 structure organization and redox behavior. Among all tested catalysts, ϵ‐MnO 2 showed the best performance with an excellent yield of 74 % of 2,5‐furandicarboxylic acid at full ‐hydroxymethylfurfural conversion. |
Author | Centeno, Miguel Ángel Álvarez-Hernández, Débora Megías-Sayago, Cristina Ivanova, Svetlana Penkova, Anna |
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Cites_doi | 10.1016/j.apcata.2014.03.020 10.1039/C9CY01968E 10.1016/j.apcata.2018.05.001 10.1002/cctc.201901742 10.1016/j.apcatb.2010.10.034 10.1021/ja1055615 10.1016/j.apcata.2016.01.005 10.1002/smll.202300394 10.1016/j.jcis.2021.02.030 10.1021/acscatal.7b01913 10.1007/s11144-014-0689-z 10.1039/D2NJ01207C 10.3390/nano7050117 10.1002/slct.201600797 10.1039/C9CY01298B 10.1016/j.est.2018.11.021 10.1021/jp0774995 10.1016/j.fuel.2020.118362 10.1002/cssc.201601443 10.1021/acssuschemeng.9b00010 10.1016/j.cattod.2018.04.024 10.1016/j.apsusc.2021.149905 10.1002/cssc.201900833 10.1021/acscatal.8b02522 10.1002/adma.202004862 10.1016/j.apcata.2012.05.016 10.1016/j.catcom.2013.12.031 10.1126/sciadv.1700782 10.1016/j.cattod.2010.03.010 10.1021/ie501098e 10.1039/c1gc15355b 10.1016/j.fuel.2022.124474 10.1039/C8GC02680G 10.1039/C6GC00438E 10.1016/j.apcatb.2019.118150 10.1021/cm00057a003 10.1016/S1872-2067(17)62922-X 10.1016/S1872-2067(17)62915-2 10.1116/11.20020401 10.3389/fchem.2020.00585 10.1016/j.apsusc.2021.150989 10.1002/jccs.201200193 10.1016/j.cattod.2020.10.037 10.1039/C7GC00027H 10.1016/j.jallcom.2018.02.260 10.1002/chem.202100478 |
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Keywords | MnO2 crystal structure 2,5-furandicarboxylic acid 5-hydroxymethylfurfural oxidation |
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References | e_1_2_8_28_1 e_1_2_8_24_1 e_1_2_8_47_1 e_1_2_8_26_1 e_1_2_8_49_1 e_1_2_8_3_1 e_1_2_8_5_1 e_1_2_8_7_1 e_1_2_8_9_1 e_1_2_8_20_1 e_1_2_8_43_1 e_1_2_8_22_1 e_1_2_8_45_1 e_1_2_8_1_1 e_1_2_8_17_1 e_1_2_8_19_1 e_1_2_8_13_1 e_1_2_8_36_1 e_1_2_8_15_1 e_1_2_8_38_1 Hayashi E. (e_1_2_8_41_1) 2019; 141 e_1_2_8_32_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_30_1 e_1_2_8_29_1 e_1_2_8_25_1 e_1_2_8_46_1 e_1_2_8_27_1 e_1_2_8_48_1 e_1_2_8_2_1 e_1_2_8_4_1 e_1_2_8_6_1 e_1_2_8_8_1 e_1_2_8_21_1 e_1_2_8_42_1 e_1_2_8_23_1 e_1_2_8_44_1 e_1_2_8_40_1 e_1_2_8_18_1 e_1_2_8_39_1 e_1_2_8_14_1 e_1_2_8_35_1 e_1_2_8_16_1 e_1_2_8_37_1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_12_1 e_1_2_8_33_1 e_1_2_8_50_1 |
References_xml | – ident: e_1_2_8_7_1 doi: 10.1016/j.apcata.2014.03.020 – ident: e_1_2_8_35_1 doi: 10.1039/C9CY01968E – ident: e_1_2_8_45_1 doi: 10.1016/j.apcata.2018.05.001 – ident: e_1_2_8_9_1 doi: 10.1002/cctc.201901742 – ident: e_1_2_8_3_1 – ident: e_1_2_8_30_1 doi: 10.1016/j.apcatb.2010.10.034 – ident: e_1_2_8_28_1 doi: 10.1021/ja1055615 – ident: e_1_2_8_31_1 doi: 10.1016/j.apcata.2016.01.005 – ident: e_1_2_8_32_1 doi: 10.1002/smll.202300394 – ident: e_1_2_8_17_1 doi: 10.1016/j.jcis.2021.02.030 – ident: e_1_2_8_46_1 doi: 10.1021/acscatal.7b01913 – ident: e_1_2_8_12_1 doi: 10.1007/s11144-014-0689-z – ident: e_1_2_8_11_1 doi: 10.1016/j.apcata.2014.03.020 – ident: e_1_2_8_10_1 doi: 10.1039/D2NJ01207C – ident: e_1_2_8_21_1 doi: 10.3390/nano7050117 – ident: e_1_2_8_42_1 doi: 10.1002/slct.201600797 – ident: e_1_2_8_16_1 doi: 10.1039/C9CY01298B – ident: e_1_2_8_19_1 doi: 10.1016/j.est.2018.11.021 – ident: e_1_2_8_25_1 doi: 10.1021/jp0774995 – ident: e_1_2_8_15_1 doi: 10.1016/j.fuel.2020.118362 – ident: e_1_2_8_18_1 doi: 10.1002/cssc.201601443 – ident: e_1_2_8_40_1 doi: 10.1021/acssuschemeng.9b00010 – ident: e_1_2_8_14_1 doi: 10.1016/j.cattod.2018.04.024 – ident: e_1_2_8_37_1 doi: 10.1016/j.apsusc.2021.149905 – ident: e_1_2_8_6_1 doi: 10.1002/cssc.201900833 – ident: e_1_2_8_50_1 doi: 10.1021/acscatal.8b02522 – ident: e_1_2_8_23_1 doi: 10.1002/adma.202004862 – ident: e_1_2_8_24_1 doi: 10.1016/j.apcata.2012.05.016 – ident: e_1_2_8_1_1 – ident: e_1_2_8_47_1 doi: 10.1016/j.catcom.2013.12.031 – ident: e_1_2_8_2_1 doi: 10.1126/sciadv.1700782 – ident: e_1_2_8_49_1 doi: 10.1016/j.cattod.2010.03.010 – ident: e_1_2_8_38_1 doi: 10.1021/ie501098e – ident: e_1_2_8_29_1 doi: 10.1039/c1gc15355b – ident: e_1_2_8_8_1 doi: 10.1016/j.fuel.2022.124474 – volume: 141 start-page: 899 year: 2019 ident: e_1_2_8_41_1 publication-title: J. Am. Chem. Soc. contributor: fullname: Hayashi E. – ident: e_1_2_8_5_1 doi: 10.1039/C8GC02680G – ident: e_1_2_8_36_1 doi: 10.1039/C6GC00438E – ident: e_1_2_8_48_1 doi: 10.1016/j.apcatb.2019.118150 – ident: e_1_2_8_26_1 doi: 10.1021/cm00057a003 – ident: e_1_2_8_44_1 doi: 10.1016/S1872-2067(17)62922-X – ident: e_1_2_8_22_1 doi: 10.1016/S1872-2067(17)62915-2 – ident: e_1_2_8_39_1 doi: 10.1116/11.20020401 – ident: e_1_2_8_4_1 doi: 10.3389/fchem.2020.00585 – ident: e_1_2_8_33_1 doi: 10.1016/j.apsusc.2021.150989 – ident: e_1_2_8_27_1 doi: 10.1002/jccs.201200193 – ident: e_1_2_8_43_1 doi: 10.1016/j.cattod.2020.10.037 – ident: e_1_2_8_13_1 doi: 10.1039/C7GC00027H – ident: e_1_2_8_20_1 doi: 10.1016/j.jallcom.2018.02.260 – ident: e_1_2_8_34_1 doi: 10.1002/chem.202100478 |
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Snippet | Noble metal-free catalyst or catalytic oxidation of 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid are proposed in this study as a proposal to solve... Abstract Noble metal‐free catalyst or catalytic oxidation of 5‐hydroxymethylfurfural into 2,5‐furandicarboxylic acid are proposed in this study as a proposal... |
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Title | Highly Effective Non-Noble MnO 2 Catalysts for 5-Hydroxymethylfurfural Oxidation to 2,5-Furandicarboxylic Acid |
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