盐酸硫脲从负载钯吸附剂中分离钯
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1.武汉科技大学 省部共建耐火材料与冶金国家重点实验室, 湖北 武汉 430081 ;2.武汉科技大学 钢铁冶金及资源利用省部共建教育部重点实验室, 湖北 武汉 430081

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张保平,王尹,张恒,等.

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TF836

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Separation of palladium from palladium-loaded adsorbent with thiourea hydrochloride
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1.State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081 , China ; 2.Key Laboratory of Iron and Steel Metallurgy and Resource Utilization, Ministry of Education, Wuhan University of Science and Technology, Wuhan 430081 , China

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    摘要:

    本研究采用盐酸和硫脲从负载钯吸附剂中分离钯,通过对反应进行热力学分析探明含钯产物的化学形态及其分布特征,揭示解吸过程机理;利用动力学模型分析解吸行为;通过试验考察时间、盐酸浓度、硫脲浓度和解吸剂体积对分离效果的影响及再生次数对吸附剂再生性能的影响。热力学分析结果表明,解吸时负载钯吸附剂中的PdCl 2-4与Cl -发生离子交换后再与硫脲配合,含钯产物以PdCl3[SC(NH2)2] -形态存在;解吸动力学分析表明,准二级动力学模型是最优模型;试验表明,在负载钯吸附剂10mg、温度25℃、解吸时间60min、解吸剂(10mol·L -1盐酸和06mol·L -1硫脲)20mL的条件下,钯的最大解吸率为9626%;吸附剂再生性结果表明,最佳的再生次数为4。

    Abstract:

    In this study, hydrochloric acid and thiourea were used to separate palladium from palladium adsorbent. Based on thermodynamic analysis of the reaction, the chemical morphology and distribution characteristics of palladium products were explored, and the mechanism of desorption process was revealed. Meanwhile, the effects of time, concentration of hydrochloric acid, concentration of thiourea and volume of desorption agent on the separation effect and the effects of regeneration times on the regeneration performance of the adsorbent were investigated. The results show that the palladium-containing products exist as PdCl3[SC(NH2)2]- after ion exchange with Cl- and thioureas in the palladium-loaded adsorbent. The quasi-second-order kinetic model is the best model for desorption kinetics. Under the conditions that the palladium-loaded adsorbent of 10mg, temperature of 25℃, desorption time of 60min, desorption agent (10mol·L -1 hydrochloric acid and 06mol·L -1 thiourea) of 20mL, the maximum desorption rate of palladium was 9626%. The results showed that the optimal regeneration times of adsorbent was 4.

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盐酸硫脲从负载钯吸附剂中分离钯[J]. 中国有色冶金, 2022, 51(4): 93-101.

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  • 收稿日期:2021-12-26
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  • 在线发布日期: 2025-12-24
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