摘要
通过溶胶-凝胶法制得了苯基聚硅氧烷,进一步磺化制备了苯基磺酸官能化的中孔硅基催化材料,并通过BET,SEM和固体核磁技术对其进行了表征.BET结果表明,该催化剂比表面积为722m2/g,平均孔径为9.06nm,孔容0.59mL/g.CCPMASNMR和SiCPMASNMR表征显示磺酸基键合于苯环间位,苯基以共价方式进入无机-有机杂化硅1329基材料的内部结构.该固体酸的活性中心磺酸基在表面呈均匀分布,在芳族羧酸和取代酚的直接酯化反应中表现出优异的催化性能.
Phenylsulfonic acid functionalized mesoporous silica as catslyst was synthesized by sol-gel technique to form a precursor bearing phenyl groups followed by further sulfonation, and characterized by BET, SEM and solid NMR. The nitrogen adsorption-desorption isotherms indicated that the specific area of the catalyst was 722 m(2)/g, the average pore size ca. 9.06 nm and pore volume 0.59 cm(3)/g. C-13 and Si-29 CPMAS NMR spectra showed that the phenyl ring bonded with sulfonic acid group in meta-position covalently interacts with the framework of the hybrid materials. With an even distribution of active sites for the sulfonic acid groups, the catalyst showed a highly catalytic performance in esterification of various aromatic carboxylic acids with substituted phenol.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2005年第5期396-400,共5页
Acta Chimica Sinica