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Microemulsion guided synthesis of microporous vanadium pentoxide.

机译:微乳液引导的微孔五氧化二钒的合成。

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We have developed a process for making microporous vanadium pentoxide that proceeds via the polymerization of vanadium isopropoxide oxide in a water/sodium dioctylsulfosuccinate (Aerosol OT)/toluene reverse microemulsion. The kinetics of this method can be separated into four steps that occur at very different speeds. The first, the reaction of alkoxide and water in the microemulsion droplets to produce polyions, takes about 100 milliseconds. The second step, the conversion of these polyions into polymer ribbons, takes about ten minutes. The third step, which involves making large clusters from the ribbons, is the slowest step, taking an hour or more. In the fourth and final step, the vanadia clusters are assembled into the final microporous structure by a sequence of washing and drying steps.; In the first step, we discovered the first order rate constant {dollar}({lcub}sim{rcub}{dollar}40 1/s) for the alkoxide-microemulsion reaction is directly related to the water concentration and inversely related to the surfactant concentration. This result is consistent with diffusion of alkoxide across a new surfactant structure formed in microemulsions containing excess surfactant.; In the second step, the sol produced above forms ribbons that are characterized by a mass fractal dimension of 2-2.4. In the third step, these ribbons aggregate into clusters, characterized by a mass fractal dimension of 2.0, over a period of an hour. The growth rate is linearly dependent on the initial alkoxide and water concentrations. This is explained by a two step process involving diffusion of the droplets and reaction of the fibers within droplets.; In the fourth and final step, three types of microporous structures from vanadium pentoxide clusters are prepared: Dense films, with little surface area; low porosity films (.27) with high surface area (100 m{dollar}sp2{dollar}/g); and high porosity films (.61) with high surface area (100 m{dollar}sp2{dollar}/g). The final film microstructure depends on the solvent from which the colloids are dried as well as the amount of surfactant present during the drying. The final porosity and surface area is created through a mechanism that involves the formation of chemical bonds during the drying step.
机译:我们已经开发了一种五氧化二钒微孔的制备方法,该方法通过在水/二辛基磺基琥珀酸钠(Aerosol OT)/甲苯反相微乳液中聚合异丙氧基氧化钒进行。该方法的动力学可以分为四个步骤,它们以非常不同的速度发生。首先,微乳液液滴中的醇盐与水反应生成聚离子需要约100毫秒。第二步,将这些聚离子转化为聚合物带,大约需要十分钟。第三步涉及用色带制作大型簇,这是最慢的一步,需要一个小时或更长时间。在第四个也是最后一个步骤中,通过一系列洗涤和干燥步骤将钒铁矿簇组装成最终的微孔结构。在第一步中,我们发现醇盐-微乳液反应的一阶速率常数{dollar}({lcub} sim {rcub} {dollar} 40 1 / s)与水浓度直接相关,与表面活性剂成反比浓度。该结果与醇盐在含有过量表面活性剂的微乳液中形成的新表面活性剂结构上的扩散一致。在第二步中,上面生产的溶胶形成带,其特征在于质量分形维数为2-2.4。在第三步中,这些色带在一个小时的时间内聚集成团,其特征为质量分形维数为2.0。生长速率线性依赖于初始醇盐和水的浓度。这可以通过两步过程来解释,该过程涉及液滴的扩散和液滴内纤维的反应。在第四步(也是最后一步)中,从五氧化二钒簇制备了三种类型的微孔结构:致密膜,表面积很小;具有高表面积(100 m {dollar} sp2 {dollar} / g)的低孔隙率薄膜(.27);高表面积(100 m {dollar} sp2 {dollar} / g)的高孔隙率薄膜(.61)。最终的膜微观结构取决于干燥胶体所用的溶剂以及干燥过程中存在的表面活性剂的量。最终的孔隙率和表面积是通过一种机制产生的,该机制涉及在干燥步骤中形成化学键。

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