溶胶-凝胶制备技术与新型催化材料Ⅲ.溶胶粒子表面修饰方法制备催化膜

提出用溶胶粒子表面修饰方法，结合溶胶凝胶技术制备无机催化膜．该方法的基本原理是利用合适的金属配合物在胶粒表面的吸附作用，经溶胶凝胶过程，将活性组分结合到无机膜中．实验测定结果表明：（ＮｉＥＤＴＡ）２－，ＶＯ－３，ＭｏＯ２－４，（Ｐｄ（ＮＨ３）４）２＋，ＰｄＣｌ２－４，ＰｔＣｌ２－６和ＲｈＣｌ３－６可用来修饰ＡｌＯＯＨ溶胶．以Ｐｄ／γＡｌ２Ｏ３催化膜的制备为例，经三次溶胶凝胶过程，可制得无裂缺的厚度为９μｍ的Ｐｄ／γＡｌ２Ｏ３催化膜，膜材料的平均孔直径为６ｎｍ，Ｐｄ被均匀地分布在膜的顶层，其平均粒径为２３ｎｍ．     

掺Eu3+硅基材料的发光性质

通过溶胶－凝胶技术制备了掺Eu^3 的硅基材料并测试了其三维荧光光谱、激光谱和发射光谱，结果显示，最佳激发波波长为350nm,最强荧光波长为620nm；在350nm光激发下的发射光谱显示Eu^3 的特征发射光谱，产生4条谱带，分别是577nm(^5D0-^7F0)，588nm(^5D0-^7F1),596nm(^5D0-^7F1)和610nm(^5D0-^7F2)。     

氢氧化铝镁正电溶胶制备及性能研究

氢氧化铝镁正电溶胶制备及性能研究侯万国，张春光，孙德军，梁晓丽，王果庭（山东大学胶体与界面化学研究所，济南，２５０１００）关键词混合金属氢氧化物，溶胶，超细颗粒混合金属氢氧化物的合成、组成及结构等已得到广泛研究［１，２］．我们也曾用插入法合成了混合金...     

Silica hybrid nanocomposites

In this work we present experimental results about the formation, properties and structure of sol — gel silica based biocomposite containing Calcium alginate as an organic compound. Two different types of silicon precursors have been used in the synthesis: tetramethylortosilicate (TMOS) and ethyltrimethoxysilane (ETMS). The samples have been prepared at room temperature. The hybrids have been synthesized by replacing different quantitis of the inorganic precursor with alginate. The structure of the obtained hybrid materials has been studied by XRD, IR Spectroscopy, EDS, BET and AFM. The results proved that all samples are amorphous possessing a surface area from 70 to 290 m²/g. It has also been established by FT IR spectra that the hybrids containing TMOS display Van der Walls and Hydrogen bonding or electrostatic interactions between the organic and inorganic components. Strong chemical bonds between the inorganic and organic components in the samples with ETMS are present. A self-organized nanostructure has been observed by AFM. In the obtained hybrids the nanobuilding blocks average in size at about 8–14 nm for the particles.     

溶胶-凝胶法制备铁酸盐超微粒子催化剂

采用溶胶－凝胶法制备了含Zn,Ni,Co的铁酸盐超微粒子催化剂，运用DTA－TG、IR、XRD以及BET比表面测试等手段对所制备的样品进行了表征。同时，考察了铁酸盐对二氧化碳选择性氧化乙苯制苯乙烯的催化性能。结果表明：制备的铁酸盐均为尖晶石型晶体，粒子的比表面积为31．9－36．3m^2/g，晶粒大小约为30－35nm，在由二氧化碳选择性氧化乙苯制苯乙烯的反应中表现出较好的催化活性。     

Development of new solid-phase microextraction fibers by sol-gel technology for the determination of organophosphorus pesticide multiresidues in food

Allyloxy bisbenzo 16-crown-5 trimethoxysilane was first used as precursor to prepare the sol-gel-derived bisbenzo crown ether/hydroxyl-terminated silicone oil (OH-TSO) SPME coating. The coating procedure involving sol solution composition and conditioning process was presented. Compared with commercial SPME stationary phases, the new coatings showed higher extraction efficiency and therefore could provide higher sensitivity for organphosphorous pesticides (OPs). Limits of detection (LODs) were in the range of 0.003-1.0 ng/g for these OPs in food samples (honey, juice, orange and pakchoi). The optimal extraction conditions of the new coatings to OPs in these samples were investigated by adjusting extraction time, salt addition, extraction temperature, and dilution ratios of samples with distilled water by using SPME coupled with gas chromatography (GC)-flame photometric detection (FPD). The method was applied to determine the concentrations of OPs in real samples.     

溶胶凝胶法制氧化铝负载铜基超细粒子催化剂的研究

采用溶胶凝胶法制氧化铝负载铜基超细粒子催化剂的制备了氧化铝负载的铜基超细粒子催化剂，用ＴＧ－ＤＴＡ，ＸＲＤ，ＢＥＴ以及ＴＥＭ等技术手段，对催化剂的物相结构，表面孔结构，粒子形貌以及催化性能等进行了研究。结果表明，利用溶胶凝胶法，可以直接帛备出高比表面积，低堆积密度的纤维状纳米级负载型Ｃｕ／Ａｌ２Ｏ３超细粒子；活性组分以远低于纳米级的微晶粒子簇状态，均匀地分散在纳米级氧化铝载体表面上，而且在低于５０     

聚丙烯/聚乙烯共混物的辐射凝胶生成动力学研究

本文研究辐照PP/HDPE共混物的溶胶生成分数s与辐照剂量R的关系,结果表明适用于某些纯聚合物辐射交联规律的Charlesby-Pinner关系式和陈-刘-唐关系式皆不适用于PP/HDPE共混体系。张万喜等人曾研究过许多纯聚合物的辐射交联,提出裂解度正比于R~β的假定,β是与高分子结构相关的参数,这个假定可与大多数聚合物的辐射交联实验数据符合。同样的假定被应用于本文的共混体系,不同的是根据共混物结构特点对R~β项进行了必要的修正,即共混物的R~β=∑f_iR~(βI),其中f_i,β_i分别为共混物第i组分的重量分数及β值。用修正后的R~β处理辐照PP/HDPE共混物的实验数据,R(s+√s)～R~β,有很好的线性关系。     

MoO3/SiO2催化剂的异丁烷选择氧化反应性能

分别采用浸渍法和溶胶－凝胶法制备了MoO3/SiO2催化剂，用XRD，TPR，IR，TPD和活性评价等手段对催化剂的影响，晶格氧活泼性，化学吸附性能和异丁烷选择氧化反应性能进行了研究。结果表明，催化剂表面由Lewis碱位Mo=M,Mo-O-Mo中的晶格氧和Lewis酸位Mo^6 构成，在MoO3/SiO2催化剂上，异丁烷主要通过甲基的H双位吸附在表面的Lewis碱位Mo=O上；在常压条件下，异丁烷选择氧化产物主要为异丁烷，甲基丙烯醛和甲基丙烯酸，其中深度氧化产物CO2主要由吸附的异丁烯继续反应生成；采用溶胶－凝胶法制备的MoO3/SiO2催化剂，可得到较高的异丁烷转化率和含氧有机物选择性。