采用浸渍法将糠醇负载在铝改性的SBA-15介孔孔道中,经550℃不完全碳化制备了结构规整、含多苯环的中空管状硅碳复合介孔材料.结果表明,通过温和磺酸化作用可使磺酸基团成功取代在多苯环上,其酸量随着多苯环涂层厚度变化在0.38~0.84mmol/g范围内可控调变.相比于蔗糖作为糖源的复合固体酸,所制碳多苯环-硅酸催化剂具有中空碳纳米管堆积的类似CMK-5介孔结构,以及较大的反应空间、稳定的机械性能、较高的比表面和大量可以接触的质子酸中心,因而在大分子缩醛(酮)反应中表现了良好的催化性能.
参考文献
[1] | Pillai S K;Gheevarghese O;Sugunan S .[J].Applied Catalysis A:General,2009,353:130. |
[2] | Katada N;Iseki Y;Shichi A;Fujita N Ishino I Osaki K Torikai T Niwa M .[J].Applied Catalysis A:General,2008,349:55. |
[3] | Shimizu K;Niimi K;Satsuma A .[J].Applied Catalysis A:General,2008,349:1. |
[4] | Atia H;Armbruster U;Martin A .Dehydration of glycerol in gas phase using heteropolyacid catalysts as active compounds[J].Journal of Catalysis,2008(1):71-82. |
[5] | Fang L;Xing R;Wu H H;Li X H Liu Y M Wu P .[J].Sci China Chem,2010,53:1481. |
[6] | 方林,张坤,李晓红,吴海虹,吴鹏.磺酸基团功能化的碳-硅介孔复合材料的制备及其在生物柴油绿色合成中的应用[J].催化学报,2012(01):114-122. |
[7] | Harmer M A;Sun Q .[J].Applied Catalysis A:General,2001,221:45. |
[8] | Saha M S;Nishiki Y;Furuta T;Denggerile A Ohsaka T .[J].Tetrahedron Letters,2003,44:5535. |
[9] | Serio M D;Tesser R;Dimiccoli M;Cammarota F Nastasi M Santacesaria E .[J].Journal of Molecular Catalysis A:Chemical,2005,239:111. |
[10] | Liu K S .[J].Journal of the American Oil Chemists'Society,1994,71:1179. |
[11] | Wang X G;Chen C C;Chen S Y;Mou Y Cheng S .[J].Applied Catalysis A:General,2005,281:47. |
[12] | Ratnama K J;Reddy R S;Sekhar N S;Kantama M L Deshpande A Figueras F .[J].Applied Catalysis A:General,2008,348:26. |
[13] | Zareyee D;Karimi B .[J].Tetrahedron Letters,2007,48:1277. |
[14] | Das B;Kanth BS;Reddy KR;Kumar AS .Sulfonic acid functionalized silica as an efficient heterogeneous recyclable catalyst for one-pot synthesis of 2-substituted benzimidazoles[J].Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry,2008(5):1499-1502. |
[15] | Barrault J;Jerome F .[J].European Journal of Lipid Science and Technology,2008,110:825. |
[16] | Saikia L;Satyarthi J K;Srinivas D;Ratnasamy P .[J].J Gatal,2007,252:148. |
[17] | Dias A S;Pillinger M;Valente A A .[J].Journal of Catalysis,2005,229:414. |
[18] | Shimizu K;Hayashi E;Hatamachi T;Kodama T Higuchi T Satsuma A Kitayama Y .[J].J Gatal,2005,231:131. |
[19] | Landge S M;Berryman M;T(o)r(o)k B .[J].Tetrahedron Letters,2008,49:4505. |
[20] | Balaraju M;Rekha V;Prasad P S S;Devi B L A P Prasad R B N Lingaiah N .[J].Applied Catalysis A:General,2009,354:82. |
[21] | Li D M;Shi F;Peng J J;Guo Sh Deng Y Q .[J].Journal of Organic Chemistry,2004,69:3582. |
[22] | Shimizu K;Hayashi E;Hatamachi T;Kodama T;Higuchi T;Satsuma A;Kitayama Y .Acidic properties of sulfonic acid-functionalized FSM-16 mesoporous silica and its catalytic efficiency for acetalization of carbonyl compounds[J].Journal of Catalysis,2005(1):131-138. |
[23] | Xing R;Liu N;Liu YM;Wu HW;Jiang YW;Chen L;He MY;Wu P .Novel solid acid catalysts: Sulfonic acid group-functionalized mesostructured polymers[J].Advanced functional materials,2007(14):2455-2461. |
[24] | Toda M;Takagaki A;Okamura M;Kondo J N Hayashi S Domen K Hara M .[J].NATURE,2005,438:178. |
[25] | Xing R;Liu Y M;Wang Y;Chen L Wu H H Jiang Y W He M Y Wu P .[J].Microporous and Mesoporous Materials,2007,105:41. |
[26] | Nakajima K;Okamura M;Kondo J N;Domen K Tatsumi T Hayashi S Hara M .[J].CHEMISTRY OF MATERIALS,2009,21:186. |
[27] | Augustine J K;Bombrun A;Sauer W H B;Vijaykumar P .[J].Tetrahedron Letters,2012,53:5030. |
[28] | Sato S;Sagara K;Furuta H;Nozaki F .[J].Journal of Molecular Catalysis A:Chemical,1996,114:209. |
[29] | Shao L J;Xing G Y;He L Y;Chen J Xie H Q Liang X Zh Qi Ch Z .[J].Applied Catalysis A:General,2012,443-444:133. |
[30] | Darmstadt H.;Roy C.;Kaliaguine S.;Kim TW.;Ryoo R. .Surface and pore structures of CMK-5 ordered mesoporous carbons by adsorption and surface spectroscopy[J].Chemistry of Materials,2003(17):3300-3307. |
[31] | Wang, Y.;Liu, Y.;Li, X.;Wu, H.;He, M.;Wu, P. .Intermolecular condensation of ethylenediamine to 1,4-diazabicyclo[2,2,2]octane over TS-1 catalysts[J].Journal of Catalysis,2009(2):258-267. |
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