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Electrosynthesis of Cobalt - Hydroxyapatite Nanoparticles

机译:钴 - 羟基磷灰石纳米粒子的电动合成

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Cobalt is one of the potential candidates that exhibit good catalyst properties. The catalyst support is needed to increase the dispersion of the catalyst and to prevent the catalyst loss. Hydroxyapatite (HA) is one of the good catalyst support for transition metal catalyst. The electrochemical synthesis to HA supported cobalt catalyst has the advantages of being easy, inexpensive, controlled, and producing metal that is perfectly dispersed at its support. The novelty of this work is the synthesis of hydroxyapatite that supports cobalt in one step by the electrochemical method. In this paper, we demonstrate the effects of current density to the particle Co-HA produced. The solution for cobalt-HA synthesis by electrochemical method is calcium chloride, potassium dihydrogen phosphate and EDTA in molar ratio 0.25/0.15/0.25 M 250 mL solution. The initial concentration of cobalt were 0.2 and 0.5 M. The cell of electrolysis consists of two carbon plates. The bipolar membrane was used to separate the electrolysis cell. The electrolysis cell had a size of (3 ×10× 10)cm and was constructed from the acrylic box. Both carbon plates were 2.5× 5 cm and placed in the electrolyte a depth of 2.5 cm. The electrolysis cell was placed in ultrasonic. The current density was various at 80, 160, and 240 mA/cm~2. The pH of the solution in the anode chamber decreased as the electrolysis time increased while in the cathode chamber increased. In the anode chamber, the higher the current density, the faster the pH of the solution decreases. In the cathode chamber, the higher the current density, the faster the pH of solution increases. The pink particles were resulted by electrolysis in the cathode chamber while no particles in the anode chamber. In the low current density, the particle products are HA and brushite while the higher current density the particle product is pure HA. The higher the current density the bigger the crystallite size of the particles.
机译:钴是具有良好催化剂性质的潜在候选者之一。需要催化剂载体来增加催化剂的分散并防止催化剂损失。羟基磷灰石(HA)是过渡金属催化剂的良好催化剂载体之一。 HA支持的钴催化剂的电化学合成具有容易,廉价,控制和生产金属的优点,其完美地分散在其载体上。这项工作的新颖性是合成羟基磷灰石,通过电化学方法在一步中支持钴。在本文中,我们证明了电流密度对产生的颗粒CO-HA的影响。通过电化学方法的钴-AH合成的溶液是氯化钙,磷酸二氢钾和EDTA,摩尔比0.25 / 0.15 / 0.25m 250mL溶液。钴的初始浓度为0.2和0.5米。电解细胞由两个碳板组成。双极膜用于分离电解槽。电解槽的尺寸为(3×10×10)cm,并由丙烯酸盒构造。两个碳板都为2.5×5cm,并置于电解质中深度为2.5厘米。电解槽置于超声波中。电流密度为80,160和240mA / cm〜2。当在阴极室中的电解时间增加时,阳极室中的溶液的pH降低。在阳极室中,电流密度越高,溶液的pH越快降低。在阴极室中,电流密度越高,溶液的pH越快增加。粉红色颗粒通过在阴极室中电解而导致,同时在阳极室中没有颗粒。在低电流密度中,颗粒产物是HA和刷石,而颗粒产物纯度纯度纯度HA。电流密度越大,颗粒的晶体尺寸越大。

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