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含表面硅羟基材料的表面改性及其在环境中的应用

Research on the Chemical Modification of Materials with Silica Hydroxy and the Application in Environment

【作者】 屈文

【导师】 苏继新;

【作者基本信息】 山东大学 , 环境工程, 2008, 硕士

【摘要】 硅胶和介孔SBA-15均是表面富含硅羟基的二氧化硅材料,本课题围绕硅胶和SBA-15的表面改性制备了HSO3-硅胶、SH-硅胶、TiO2/SBA-15、Au-Ti/SBA-15,并将其应用于相应的催化反应中。以氯丙基氯硅烷和苯基氯硅烷对硅胶进行表面改性,进一步磺化得到以磺酸基为活性中心的固体酸,磺化剂分别为硫酸和亚硫酸铵。以BET、红外光谱、总有机碳对固体酸及其前驱体进行了表征并测定了固体酸酸密度;利用总有机碳计算前驱体的键合量,苯基、氯丙基硅胶键合量分别为1.40mmol/g、1.95mmol/g;以这两种前驱体制得的固体酸酸密度分别为0.32mmol/g、0.26mmol/g;BET数据表明键合反应发生后样品的比表面积变小。将制得固体酸应用于乙酸丁酯的合成,结果表明催化剂使用寿命较长,转化率和选择性较高。采用表面化学改性的方法将廉价氯丙基引入到硅胶表面,以硫氢化钠进一步改性得巯基硅胶,用BET、TOC、红外光谱、元素分析对巯基硅胶及其前驱体结构进行了表征,结果表明此制备方法得到巯基含量为1.56mmol/的材料。将所得巯基硅胶应用于含汞废水的去除和含贵金属废水的回收中,吸附实验结果表明对于Hg2+、Pd2+、Au3+材料饱和吸附量分别为47mg/L、87mg/g、120mg/g,且在干扰离子存在时,样品表现了良好的选择性。将硫酸钛浸渍到SBA-15孔道中,经升温原位沉淀、焙烧得到纳米孔道中均匀分散的锐钛型二氧化钛。用TEM、BET、XRD、SAXD、UV-Vis漫反射吸收光谱等方法对材料进行了表征。结果表明,改性后的SBA-15仍保持着有序的孔道,二氧化钛颗粒较均匀地分布在SBA-15孔道内部,SBA-15合适的纳米孔道对二氧化钛颗粒的长大起到较好的限制作用;紫外光下的甲基橙光降解结果表明,SBA-15负载的纳米二氧化钛颗粒有优于商品P25的光催化性能。用无水氯化物气相键合法对介孔材料进行了修饰,将Ti、Mo成功键合到SBA-15表面,并用BET、HRTEM、UV-Vis漫反射吸收光谱对材料进行了表征,结果表明金属氧化物以单层的方式均匀键合在孔道内部。以CO氧化实验为探针考察了Au-Ti/SBA-15的催化活性,结果表明材料在较宽温度范围内具有良好活性,SBA-15孔道对金颗粒聚集有较好限制作用。

【Abstract】 Silica-gel and mesoporous SBA-15 are both silica oxide material with abundance of suraface Si-OH.HSO3-silica、SH-silica、TiO2/SBA-15、Au-Ti2O-SBA-15 were sybthesised by surface modification method,and these materials were applied in different catalysis rection。The phenyl and chloropropyl silica derived from chlorosilane were applied to synthesize HSO3-functionalized silica by using H2SO4 or(NH42SO3.The solid acid and their precursors were characterized by BET,IR,TOC.The surface coverage density of phenyl-silica and chloropropyl-silica were 1.40mmol/g and1.95mmol/g, while the acid exchanger capacities are 0.32mmol/g and 0.26mmol/g,respectively. The specific area of the samples decreased from 511m2/g to 406 m2/g and 432 m2/g. The solid acids were used in the synthesis of butyl acetate,and the results indicated that the catalysts can be reused for 5 times with high conversion.Thiol-functionalized silica has been prepared by cheaper chloropropyl trichlorosilane and NaSH successfully instead of expensive mercaptosilylating agent. The silica-SH and its precursor are characterized by BET,FT-IR,TOC and element analysis.Surface coverage density of silica-chloropropyl and silica-SH is 2.5mmol/g and1.56mmol/g,respectively.The silica-SH is used as sorbent to fix heavy metal ions,and the saturated adsorption capacity for Hg2+,Pd2+,Au3+were 47mg/L、87mg/g、120mg/g respectively,so it is an excellence material for fixation of mercury from wastewater and waste solid.Nanocrystalline anatase TiO2 limited within the mesoporous channels of SBA-15 has been prepared by in-situ hydrolysis precipitation of Ti(SO42 solution and calcination subsequently.The as-synthesized samples were characterized by TEM, BET,XRD,SAXD,Raman,UV-Vis,XPS,XRF techniques,and the results indicated that nano-TiO2 particles were restricted within the channel and dispersed uniformly without block the pores.The Raman and XPS data indicated that most TiO2 particles are deposited on the support without forming Ti-O-Si bond.The activities of the samples were evaluated by the photo degradation of methyl orange under UV-light.The results showed that the TiO2 contents and the size of particles on the support of SBA-15 affected the catalytic activity obviously,and the samples with TiO2 particles size about 6~7nm showed the best catalytic activity.Little difference of the activity was observed between the fresh sample and the sample used for 5 times.TiO2 and Mo2O3 were attach to the surface of SBA-15 by gas-phase surface modification using their chloride as precursors.The samples are characterized by BET, HRTEM,UV-Vis diffuse reflection absorption spectrum.The results indicated that Ti、Mo are in the channel of the SBA-15 without block it.The Au/Ti-SBA-15 are used to used in the oxidation of CO,and the results indicated that the catalysts in a wide range of temperature and the SBA-15 confined the growth of Au particles.

  • 【网络出版投稿人】 山东大学
  • 【网络出版年期】2009年 01期
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