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首页> 外文期刊>Ultrasonics sonochemistry >In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach
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In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach

机译:作为一种新型吸附剂的体外合成,用于从地下水中除去氟离子:超声波方法

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Marble waste powder consisting of calcium and magnesium compounds was used to synthesize a novel bio-compatible product, marble apatite (MA) primarily hydroxyapatite (Hap) for applications in defluoridation of drinking water. Synthesis of marble apatite was carried out by using calcium compounds (mixture of hydroxide and nitrate) extracted from marble waste powder which was treated with potassium dihydrogen phosphate at 80 degrees C under alkaline conditions using conventional precipitation method (CM) and ultrasonication method (USM). Qualitative analysis of synthesized marble apatite from both the methods was carried out using FTIR, phase analysis by XRD and microstructure analysis by SEM and TEM. When ultrasonication (USM) method was used, the yield of marble apatite was improved from 67.5% to 78.4%, with reduction in crystallite size (58.46 nm), lesser agglomeration and comparatively well-defined spherical morphology compared to the CM method. Studies also include estimation of the defluoridation capacity of MA as an adsorbent for drinking water treatment and effects of process parameters such as pH, contact time, initial fluoride concentration, dosage and presence of other co-ions on fluoride removal capacity. The results showed that the experimental adsorption capacity of the marble apatite synthesized using USM method was significantly higher (1.826 mg/g) than marble apatite synthesized using conventional method (0.96 mg/g) at pH 7 with a contact time of 90 min. The mechanism of adsorption was studied, and it was observed that Langmuir isotherm model fitted best to the experimental data, while the kinetic studies revealed that the process followed pseudo-second order model.
机译:由钙和镁化合物组成的大理石废粉用于合成新的生物相容产品,主要是羟基磷灰石(HAP),以便在饮用水的偏氟中应用。通过使用常规沉淀法(CM)(CM)和超声处理(USM)在80℃下在80℃下在80℃下在80℃下用磷酸钾处理的大理石废粉化合物(氢氧化物和硝酸盐)进行摩尔磷灰石的合成。 。使用FTIR,通过SEM和TEM通过XRD和微观结构分析来进行来自两种方法的合成大理石磷灰石的定性分析。当使用超声(USM)方法时,大理石磷灰石的产率从67.5%提高到78.4%,减少微晶尺寸(58.46nm),与CM法相比,较少的附聚和相对明确定义的球形形态。研究还包括估计MA作为吸附剂的吸附剂的渗透能力,用于饮用水处理和工艺参数的影响,例如pH,接触时间,初始氟化物浓度,剂量和其他共同离子的存在对氟化物去除能力。结果表明,使用USM方法合成的大理石磷灰石的实验吸附能力明显高于(1.826mg / g),比在pH7的常规方法(0.96mg / g)在pH7中合成的大理石磷灰石,其接触时间为90分钟。研究了吸附机理,观察到Langmuir等温模型最适合实验数据,而动力学研究表明,该过程跟随伪二阶模型。

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