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在 Al(OH)(3)·Cr(OH)(3)纳米颗粒存在下过氯酸铵的热分解。

Thermal decomposition of ammonium perchlorate in the presence of Al(OH)(3)·Cr(OH)(3) nanoparticles.

机构信息

Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; National Engineering Laboratory for Hydrometallurgical Cleaner Production Technology, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; University of Chinese Academy of Sciences, Beijing 100049, China.

Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China; National Engineering Laboratory for Hydrometallurgical Cleaner Production Technology, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

J Hazard Mater. 2014 Mar 15;268:273-80. doi: 10.1016/j.jhazmat.2014.01.016. Epub 2014 Jan 19.

Abstract

An Al(OH)(3)·Cr(OH)(3) nanoparticle preparation procedure and its catalytic effect and mechanism on thermal decomposition of ammonium perchlorate (AP) were investigated using transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis and differential scanning calorimetry (TG-DSC), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis and mass spectroscopy (TG-MS). In the preparation procedure, TEM, SAED, and FT-IR showed that the Al(OH)(3)·Cr(OH)(3) particles were amorphous particles with dimensions in the nanometer size regime containing a large amount of surface hydroxyl under the controllable preparation conditions. When the Al(OH)(3)·Cr(OH)(3) nanoparticles were used as additives for the thermal decomposition of AP, the TG-DSC results showed that the addition of Al(OH)(3)·Cr(OH)(3) nanoparticles to AP remarkably decreased the onset temperature of AP decomposition from approximately 450°C to 245°C. The FT-IR, RS and XPS results confirmed that the surface hydroxyl content of the Al(OH)(3)·Cr(OH)(3) nanoparticles decreased from 67.94% to 63.65%, and Al(OH)3·Cr(OH)3 nanoparticles were limitedly transformed from amorphous to crystalline after used as additives for the thermal decomposition of AP. Such behavior of Al(OH)(3)·Cr(OH)(3) nanoparticles promoted the oxidation of NH3 of AP to decompose to N2O first, as indicated by the TG-MS results, accelerating the AP thermal decomposition.

摘要

采用透射电子显微镜(TEM)、X 射线衍射(XRD)、热重分析和差示扫描量热法(TG-DSC)、X 射线光电子能谱(XPS)和热重分析和质谱(TG-MS)研究了 Al(OH)(3)·Cr(OH)(3)纳米颗粒的制备方法及其对高氯酸铵(AP)热分解的催化作用和机理。在制备过程中,TEM、SAED 和 FT-IR 表明,在可控的制备条件下,Al(OH)(3)·Cr(OH)(3)颗粒是具有纳米尺寸的无定形颗粒,含有大量表面羟基。当 Al(OH)(3)·Cr(OH)(3)纳米颗粒用作 AP 热分解的添加剂时,TG-DSC 结果表明,AP 分解的起始温度从约 450°C 显著降低至 245°C。FT-IR、RS 和 XPS 结果证实,Al(OH)(3)·Cr(OH)(3)纳米颗粒的表面羟基含量从 67.94%降低至 63.65%,并且 Al(OH)3·Cr(OH)3 纳米颗粒在用作 AP 热分解的添加剂后从无定形有限转化为结晶。这种 Al(OH)(3)·Cr(OH)(3)纳米颗粒的行为促进了 AP 中 NH3 的氧化,首先分解为 N2O,这一点可以从 TG-MS 结果中得到证实,从而加速了 AP 的热分解。

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