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Thermal decomposition of metatitanic acid and its application as a heavy metal adsorbent

机译:偏钛酸的热分解及其在重金属吸附剂中的应用

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Thermal decomposition of metatitanic acid and its application as a heavy metal adsorbent One-dimensional (1D) nanostructured inorganic materials (nanowires, nanorods, or nanotubes) are interesting from various aspects. Such structures can be considered as building blocks for sensors, electronics, photonics, and bioelectronics applications. Their potential relies on the subtle control of their physical properties, which are based on their atomic scale structures, and their 1D morphology, i.e., their length and diameter dimensions at the nano- and microscale. By controlling these parameters, a variety of chemical and physical properties can be tailoredl. A unique way of synthesis of advanced materials via extraction of sulfate ions from the crystals of titanyl sulfate and their replacement with hydroxyl groups leaving the Ti-O framework untouched has been proposed2,3. The particle size and morphology of the starting hydrated titanyl sulfate is well preserved in the pseudomorphs of amorphous metatitanic acid including such details like the layered structure of the original hydrated titanyl sulfate crystals. The thermal transformations of metatitanic acid with rod-shaped structure were followed by simultaneous TG/DTA measurements at different heating rates with simultaneous analysis of evolved gases. The first step is characterized as the water and carbon dioxide loss. The second step is represented by the evolution of residual water. In the third step, a sharp exothermic peak representing the crystallization of anatase can be seen (as evidenced by XRD). This phase transition is also accompanied with a small mass loss that can be explained by the opening of cavities and evolution of captured gases at the temperature of crystallization. Then, the potential of adsorptive removal of Pb(II) ions from aqueous environment was investigated. It was observed that with the increasing initial lead(II) ion concentration from 1-10 mM, the maximum adsorption capacities increased gradually. The kinetic experiments showed that the time necessary to reach equilibrium is less than 60 minutes. The maximum adsorbed amount for Pb(II) as calculated from the Langmuir adsorption model was 3.4 mmol g-1. The influence of annealing temperature of prepared material on sorption of Pb(II) was tested with a result that prepared sample seems to be high efficient sorbent. However, the higher the annealing temperature the lower the adsorbed amount of heavy metal ions. Combining the results of adsorption experiments with material characteristics leads to conclusion that the heavy metal ions adsorption efficiency increase with decreasing degree of crystallinity.
机译:从各个方面来看,偏钛酸的热分解及其作为重金属吸附剂的应用一维(1D)纳米结构化无机材料(纳米线,纳米棒或纳米管)引起了人们的兴趣。这样的结构可以被认为是传感器,电子,光子学和生物电子应用的构建块。它们的潜力取决于对它们物理性质的微妙控制,这是基于它们的原子尺度结构及其一维形态,即它们在纳米和微米尺度上的长度和直径尺寸。通过控制这些参数,可以调整各种化学和物理性质。有人提出了一种独特的合成方法,该方法是通过从钛氧基硫酸钛的晶体中提取硫酸根离子并用羟基取代而保持Ti-O骨架不受影响的方式合成高级离子[2,3]。在无定形偏钛酸的假晶型中很好地保留了起始水合硫酸氧钛硫酸盐的粒径和形态,包括诸如原始水合硫酸氧钛硫酸盐晶体的层状结构之类的细节。具有棒状结构的偏钛酸的热转化,随后在不同的加热速率下同时进行TG / DTA测量,同时分析析出的气体。第一步的特征是水和二氧化碳的损失。第二步以残留水的释放为代表。在第三步中,可以看到代表锐钛矿结晶的尖锐的放热峰(由XRD证实)。这种相变还伴随着少量的质量损失,这可以通过开孔和结晶温度下捕获气体的释放来解释。然后,研究了从水性环境中吸附去除Pb(II)离子的潜力。观察到随着初始铅(II)离子浓度从1-10 mM增加,最大吸附容量逐渐增加。动力学实验表明达到平衡所需的时间少于60分钟。由Langmuir吸附模型计算出的Pb(II)的最大吸附量为3.4 mmol g-1。测试了制得材料的退火温度对Pb(II)吸附的影响,结果制得的样品似乎是高效吸附剂。但是,退火温度越高,重金属离子的吸附量越低。将吸附实验的结果与材料特性相结合,得出结论,重金属离子的吸附效率随结晶度的降低而增加。

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