One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer
Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the ave...
Ausführliche Beschreibung
Autor*in: |
Adam, Farook [verfasserIn] Batagarawa, Muazu Samaila [verfasserIn] Hello, Kasim Mohammed [verfasserIn] Al-Juaid, Salih S. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2012 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Chemical papers - Wien : Springer Vienna, 1947, 66(2012), 11 vom: 11. Sept., Seite 1048-1058 |
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Übergeordnetes Werk: |
volume:66 ; year:2012 ; number:11 ; day:11 ; month:09 ; pages:1048-1058 |
Links: |
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DOI / URN: |
10.2478/s11696-012-0203-x |
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Katalog-ID: |
SPR021868158 |
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245 | 1 | 0 | |a One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
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520 | |a Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. | ||
650 | 4 | |a surface modification |7 (dpeaa)DE-He213 | |
650 | 4 | |a sol-gel |7 (dpeaa)DE-He213 | |
650 | 4 | |a sulfonic acid |7 (dpeaa)DE-He213 | |
650 | 4 | |a glycerol |7 (dpeaa)DE-He213 | |
650 | 4 | |a acetalization |7 (dpeaa)DE-He213 | |
650 | 4 | |a -5-hydroxy-2-phenyl-1,3-dioxane |7 (dpeaa)DE-He213 | |
700 | 1 | |a Batagarawa, Muazu Samaila |e verfasserin |4 aut | |
700 | 1 | |a Hello, Kasim Mohammed |e verfasserin |4 aut | |
700 | 1 | |a Al-Juaid, Salih S. |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Chemical papers |d Wien : Springer Vienna, 1947 |g 66(2012), 11 vom: 11. Sept., Seite 1048-1058 |w (DE-627)518347737 |w (DE-600)2252770-9 |x 1336-9075 |7 nnns |
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10.2478/s11696-012-0203-x doi (DE-627)SPR021868158 (SPR)s11696-012-0203-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Adam, Farook verfasserin aut One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 Batagarawa, Muazu Samaila verfasserin aut Hello, Kasim Mohammed verfasserin aut Al-Juaid, Salih S. verfasserin aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 66(2012), 11 vom: 11. Sept., Seite 1048-1058 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 https://dx.doi.org/10.2478/s11696-012-0203-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 66 2012 11 11 09 1048-1058 |
spelling |
10.2478/s11696-012-0203-x doi (DE-627)SPR021868158 (SPR)s11696-012-0203-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Adam, Farook verfasserin aut One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 Batagarawa, Muazu Samaila verfasserin aut Hello, Kasim Mohammed verfasserin aut Al-Juaid, Salih S. verfasserin aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 66(2012), 11 vom: 11. Sept., Seite 1048-1058 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 https://dx.doi.org/10.2478/s11696-012-0203-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 66 2012 11 11 09 1048-1058 |
allfields_unstemmed |
10.2478/s11696-012-0203-x doi (DE-627)SPR021868158 (SPR)s11696-012-0203-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Adam, Farook verfasserin aut One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 Batagarawa, Muazu Samaila verfasserin aut Hello, Kasim Mohammed verfasserin aut Al-Juaid, Salih S. verfasserin aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 66(2012), 11 vom: 11. Sept., Seite 1048-1058 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 https://dx.doi.org/10.2478/s11696-012-0203-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 66 2012 11 11 09 1048-1058 |
allfieldsGer |
10.2478/s11696-012-0203-x doi (DE-627)SPR021868158 (SPR)s11696-012-0203-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Adam, Farook verfasserin aut One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 Batagarawa, Muazu Samaila verfasserin aut Hello, Kasim Mohammed verfasserin aut Al-Juaid, Salih S. verfasserin aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 66(2012), 11 vom: 11. Sept., Seite 1048-1058 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 https://dx.doi.org/10.2478/s11696-012-0203-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 66 2012 11 11 09 1048-1058 |
allfieldsSound |
10.2478/s11696-012-0203-x doi (DE-627)SPR021868158 (SPR)s11696-012-0203-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Adam, Farook verfasserin aut One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 Batagarawa, Muazu Samaila verfasserin aut Hello, Kasim Mohammed verfasserin aut Al-Juaid, Salih S. verfasserin aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 66(2012), 11 vom: 11. Sept., Seite 1048-1058 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 https://dx.doi.org/10.2478/s11696-012-0203-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 66 2012 11 11 09 1048-1058 |
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Enthalten in Chemical papers 66(2012), 11 vom: 11. Sept., Seite 1048-1058 volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 |
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Enthalten in Chemical papers 66(2012), 11 vom: 11. Sept., Seite 1048-1058 volume:66 year:2012 number:11 day:11 month:09 pages:1048-1058 |
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surface modification sol-gel sulfonic acid glycerol acetalization -5-hydroxy-2-phenyl-1,3-dioxane |
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Adam, Farook @@aut@@ Batagarawa, Muazu Samaila @@aut@@ Hello, Kasim Mohammed @@aut@@ Al-Juaid, Salih S. @@aut@@ |
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2012-09-11T00:00:00Z |
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BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. 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author |
Adam, Farook |
spellingShingle |
Adam, Farook ddc 540 bkl 35.00 misc surface modification misc sol-gel misc sulfonic acid misc glycerol misc acetalization misc -5-hydroxy-2-phenyl-1,3-dioxane One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
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540 - Chemistry & allied sciences |
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1336-9075 |
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540 ASE 35.00 bkl One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer surface modification (dpeaa)DE-He213 sol-gel (dpeaa)DE-He213 sulfonic acid (dpeaa)DE-He213 glycerol (dpeaa)DE-He213 acetalization (dpeaa)DE-He213 -5-hydroxy-2-phenyl-1,3-dioxane (dpeaa)DE-He213 |
topic |
ddc 540 bkl 35.00 misc surface modification misc sol-gel misc sulfonic acid misc glycerol misc acetalization misc -5-hydroxy-2-phenyl-1,3-dioxane |
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ddc 540 bkl 35.00 misc surface modification misc sol-gel misc sulfonic acid misc glycerol misc acetalization misc -5-hydroxy-2-phenyl-1,3-dioxane |
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ddc 540 bkl 35.00 misc surface modification misc sol-gel misc sulfonic acid misc glycerol misc acetalization misc -5-hydroxy-2-phenyl-1,3-dioxane |
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One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
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(DE-627)SPR021868158 (SPR)s11696-012-0203-x-e |
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One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
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Adam, Farook |
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Adam, Farook Batagarawa, Muazu Samaila Hello, Kasim Mohammed Al-Juaid, Salih S. |
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one-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
title_auth |
One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
abstract |
Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. |
abstractGer |
Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. |
abstract_unstemmed |
Abstract A one-pot method was employed to immobilize sulfonic acid onto silica obtained from rice husk ash using 3-(mercaptopropyl)trimethoxysilane to form a solid catalyst denoted as $ RHASO_{3} $H. BET measurements of the catalyst showed the surface area to be 340 $ m^{2} $ $ g^{−1} $ with the average pore volume of 0.24 mL $ g^{−1} $ and the pore diameter of 2.9 nm. Acidity test of cation exchange capacity and pyridine adsorption studies revealed the presence of Brønsted acid sites on the catalyst surface. The catalyst was used in the acetalization reaction of glycerol with benzaldehyde. Under optimized conditions, the reaction showed the maximum conversion of 78 % after 8 h with 67 % selectivity towards the five membered ring isomer. Variation in the glycerol concentration had a significant effect on the reactants conversion. A single crystal X-ray study of one of the products proved the existence of a unique trimer formed by hydrogen bonding by the six-membered cis-isomer. The catalyst was several times recycled without any loss of its catalytic activity. |
collection_details |
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container_issue |
11 |
title_short |
One-step synthesis of solid sulfonic acid catalyst and its application in the acetalization of glycerol: crystal structure of cis-5-hydroxy-2-phenyl-1,3-dioxane trimer |
url |
https://dx.doi.org/10.2478/s11696-012-0203-x |
remote_bool |
true |
author2 |
Batagarawa, Muazu Samaila Hello, Kasim Mohammed Al-Juaid, Salih S. |
author2Str |
Batagarawa, Muazu Samaila Hello, Kasim Mohammed Al-Juaid, Salih S. |
ppnlink |
518347737 |
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isOA_txt |
false |
hochschulschrift_bool |
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doi_str |
10.2478/s11696-012-0203-x |
up_date |
2024-07-04T00:47:20.214Z |
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|
score |
7.400589 |