{"title":"在氧化铝上一锅法合成约束结构Ru3Sn7合金,用于糠醇快速选择性氢解制1,5-戊二醇†","authors":"Rodiansono , Atina Sabila Azzahra , Edi Mikrianto , Kiky Corneliasari Sembiring , Ahmad Afandi , Gagus Ketut Sunnardianto , Indri Badria Adilina","doi":"10.1039/d5cy00542f","DOIUrl":null,"url":null,"abstract":"<div><div>A facile one-pot synthesis of confined structure Ruthenium–tin alloy catalysts on alumina ((op)Ru–(<em>x</em>)Sn@Al<sub>2</sub>O<sub>3</sub>) has been developed for highly efficient and selective synthesis of 1,5-pentanediol (1,5-PeD) from furfuryl alcohol (FFalc). A series of (op)Ru–(<em>x</em>)Sn@Al<sub>2</sub>O<sub>3</sub> (<em>x</em> = Sn co-loading; 0.37–2.65 wt%) catalysts were synthesised <em>via</em> a one-pot coprecipitation-hydrothermal method of a solution containing ruthenium chloride and tin chloride and a hydrargillite-type of aluminium hydroxide (Al(OH)<sub>3</sub>) at <span>150 °C</span> for <span>24</span> h, followed by reduction with H<sub>2</sub> at <span>400 °C</span> for 2 h. The (op)Ru–(1.30)Sn@Al<sub>2</sub>O<sub>3</sub> catalyst obviously allowed the highest yield of 1,5-PeD (97%) with a productivity of <span>3.67</span> mmol <span>1,5-</span>PeD per g<sub>cat</sub>.per min from FFalc in water at 140 °C and 10 bar H<sub>2</sub>, after 3 h. The presence of Ru<sub>3</sub>Sn<sub>7</sub> or Ru–SnO<sub><em>x</em></sub> catalysed the partial hydrogenation of the furan ring of FFalc to form 4,5-dihydrofuranmethanol (<span>4,5-DHFM</span>), and the acidic species of SnO<sub><em>x</em></sub> or Sn<sup><em>n</em>+</sup> or acidic Al<sub>2</sub>O<sub>3</sub> were used for activating C2–O for ring opening processes, while Ru<sup>0</sup> was used for the subsequent hydrogenation process, leading to high yield of the final 1,5-PeD product<span>.</span> This is the highest reported yield of 1,5-PeD from one-pot hydrogenolysis of FFalc under mild conditions<span>. C</span>atalytic performance of the recycled (op)Ru–(1.30)Sn@<span>Al</span><sub><span>2</span></sub><span>O</span><sub><span>3</span></sub> catalyst was restored after reactivation with H<sub>2</sub> at 400 °C for 1 h.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 18","pages":"Pages 5452-5463"},"PeriodicalIF":4.2000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"One-pot synthesis of confined structure Ru3Sn7 alloys on alumina for exceptionally rapid and selective hydrogenolysis of furfuryl alcohol to 1,5-pentanediol†\",\"authors\":\"Rodiansono , Atina Sabila Azzahra , Edi Mikrianto , Kiky Corneliasari Sembiring , Ahmad Afandi , Gagus Ketut Sunnardianto , Indri Badria Adilina\",\"doi\":\"10.1039/d5cy00542f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A facile one-pot synthesis of confined structure Ruthenium–tin alloy catalysts on alumina ((op)Ru–(<em>x</em>)Sn@Al<sub>2</sub>O<sub>3</sub>) has been developed for highly efficient and selective synthesis of 1,5-pentanediol (1,5-PeD) from furfuryl alcohol (FFalc). A series of (op)Ru–(<em>x</em>)Sn@Al<sub>2</sub>O<sub>3</sub> (<em>x</em> = Sn co-loading; 0.37–2.65 wt%) catalysts were synthesised <em>via</em> a one-pot coprecipitation-hydrothermal method of a solution containing ruthenium chloride and tin chloride and a hydrargillite-type of aluminium hydroxide (Al(OH)<sub>3</sub>) at <span>150 °C</span> for <span>24</span> h, followed by reduction with H<sub>2</sub> at <span>400 °C</span> for 2 h. The (op)Ru–(1.30)Sn@Al<sub>2</sub>O<sub>3</sub> catalyst obviously allowed the highest yield of 1,5-PeD (97%) with a productivity of <span>3.67</span> mmol <span>1,5-</span>PeD per g<sub>cat</sub>.per min from FFalc in water at 140 °C and 10 bar H<sub>2</sub>, after 3 h. The presence of Ru<sub>3</sub>Sn<sub>7</sub> or Ru–SnO<sub><em>x</em></sub> catalysed the partial hydrogenation of the furan ring of FFalc to form 4,5-dihydrofuranmethanol (<span>4,5-DHFM</span>), and the acidic species of SnO<sub><em>x</em></sub> or Sn<sup><em>n</em>+</sup> or acidic Al<sub>2</sub>O<sub>3</sub> were used for activating C2–O for ring opening processes, while Ru<sup>0</sup> was used for the subsequent hydrogenation process, leading to high yield of the final 1,5-PeD product<span>.</span> This is the highest reported yield of 1,5-PeD from one-pot hydrogenolysis of FFalc under mild conditions<span>. C</span>atalytic performance of the recycled (op)Ru–(1.30)Sn@<span>Al</span><sub><span>2</span></sub><span>O</span><sub><span>3</span></sub> catalyst was restored after reactivation with H<sub>2</sub> at 400 °C for 1 h.</div></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"15 18\",\"pages\":\"Pages 5452-5463\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475325003661\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475325003661","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
One-pot synthesis of confined structure Ru3Sn7 alloys on alumina for exceptionally rapid and selective hydrogenolysis of furfuryl alcohol to 1,5-pentanediol†
A facile one-pot synthesis of confined structure Ruthenium–tin alloy catalysts on alumina ((op)Ru–(x)Sn@Al2O3) has been developed for highly efficient and selective synthesis of 1,5-pentanediol (1,5-PeD) from furfuryl alcohol (FFalc). A series of (op)Ru–(x)Sn@Al2O3 (x = Sn co-loading; 0.37–2.65 wt%) catalysts were synthesised via a one-pot coprecipitation-hydrothermal method of a solution containing ruthenium chloride and tin chloride and a hydrargillite-type of aluminium hydroxide (Al(OH)3) at 150 °C for 24 h, followed by reduction with H2 at 400 °C for 2 h. The (op)Ru–(1.30)Sn@Al2O3 catalyst obviously allowed the highest yield of 1,5-PeD (97%) with a productivity of 3.67 mmol 1,5-PeD per gcat.per min from FFalc in water at 140 °C and 10 bar H2, after 3 h. The presence of Ru3Sn7 or Ru–SnOx catalysed the partial hydrogenation of the furan ring of FFalc to form 4,5-dihydrofuranmethanol (4,5-DHFM), and the acidic species of SnOx or Snn+ or acidic Al2O3 were used for activating C2–O for ring opening processes, while Ru0 was used for the subsequent hydrogenation process, leading to high yield of the final 1,5-PeD product. This is the highest reported yield of 1,5-PeD from one-pot hydrogenolysis of FFalc under mild conditions. Catalytic performance of the recycled (op)Ru–(1.30)Sn@Al2O3 catalyst was restored after reactivation with H2 at 400 °C for 1 h.
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