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Preparation and characteristics of FePO_4·xH_2O powder

机译:FePO_4·xH_2O粉体的制备及性能

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Nano-sized precursor FePO_4·xH_2O particles were obtained by oxidation co-precipitation using FeSO_4·7H_2O, H_2O_2 and ammonia. The powder was characterized by differential thermal analysis (DTA) and thermogravimetry (TG), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The TG-DTA results determined the content of crystal water of FePO_4·xH_2O, i.e. x = 1.5. The SEM observation suggested that FePO_4·xH_2O particles were spherical in shape and its grain size was about 150 nanometers. The dispersion of the synthesized powder was improved through the addition of surfactant. The XRD analysis indicated that the synthesized FePO_4·xH_2O was amorphous. After being calcined at 720 °C for 10 hrs, the synthesized FePO_4·xH_2O at pH of ~3.5 was crystallized and FePO_4 in a single phase was obtained. According to the test results, the optimized preparation process parameters were determined.
机译:通过使用FeSO_4·7H_2O,H_2O_2和氨水进行氧化共沉淀,获得了纳米级前体FePO_4·xH_2O颗粒。通过差热分析(​​DTA)和热重分析(TG),扫描电子显微镜(SEM)和X射线衍射(XRD)对粉末进行表征。 TG-DTA结果确定了FePO_4·xH_2O的结晶水含量,即x = 1.5。 SEM观察表明,FePO_4·xH_2O颗粒为球形,粒径约为150纳米。通过添加表面活性剂改善了合成粉末的分散性。 XRD分析表明合成的FePO_4·xH_2O为非晶态。在720°C下煅烧10小时后,使合成的FePO_4·xH_2O在pH值为3.5时结晶,并获得单相FePO_4。根据测试结果,确定了优化的制备工艺参数。

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