Selection of sorption materials for the extraction of nickel and cobalt from the ore of the Gornostaevskoye deposit

IF 0.3 Q4 CHEMISTRY, MULTIDISCIPLINARY
Yelena Panova, Y. Aubakirov, H. Arbag
{"title":"Selection of sorption materials for the extraction of nickel and cobalt from the ore of the Gornostaevskoye deposit","authors":"Yelena Panova, Y. Aubakirov, H. Arbag","doi":"10.15328/cb1180","DOIUrl":null,"url":null,"abstract":"Oxidized nickel ores account for the majority of industrial ores suitable for nickel production. The processing of such ores using traditional pyrometallurgical technology is not economically viable due to the low nickel content. One of the most cost-effective methods of processing oxidized nickel ores is sulfuric acid leaching technology followed by sorption extraction. The aim of this work is to establish the kinetic and thermodynamic parameters of the sorption extraction of nickel and cobalt using iminodiacetate chelating ion-exchange sorbents from various manufacturers, to select a desorbing solution and to determine the degree of desorption. The sorption of nickel and cobalt was carried out in a weakly acidic medium from a model solution containing impurities of other metals in static and dynamic modes. The limiting sorption capacity for the studied sorbents is 18-26 mg/g for nickel and 1-2 mg/g for cobalt in the static mode. The sorption capacity in the dynamic mode for nickel is equal to 25.5 g/L for Purolite S 930, 29.2 g/L for Lewatit TP 207, 1.4 g/L, and 1.8 g/L for cobalt, respectively. The best desorption parameters are achieved when using a 2 M sulfuric acid solution. The degree of desorption for sorbents Purolite S 930 and Lewatit TP 207 exceeds 90%. The use of the Lewatit TP 207 sorbent for the extraction of nickel from the leaching solution of nickel ore of the Gornostaevskoye deposit in 5 cycles made it possible to obtain a commercial desorbate with a nickel content of 18 g/L. The use of a part of the commercial desorbate obtained in the previous cycle, further strengthened to the initial concentration of sulfuric acid, for re-extracting nickel from the saturated sorbent during a cyclic process leads to a deterioration in desorption characteristics. It is recommended to remove the commercial desorbate from the process after several cycles of desorption and supply new solution of sulfuric acid for desorption to restore the sorption parameters.","PeriodicalId":9860,"journal":{"name":"Chemical Bulletin of Kazakh National University","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2021-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Bulletin of Kazakh National University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15328/cb1180","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 2

Abstract

Oxidized nickel ores account for the majority of industrial ores suitable for nickel production. The processing of such ores using traditional pyrometallurgical technology is not economically viable due to the low nickel content. One of the most cost-effective methods of processing oxidized nickel ores is sulfuric acid leaching technology followed by sorption extraction. The aim of this work is to establish the kinetic and thermodynamic parameters of the sorption extraction of nickel and cobalt using iminodiacetate chelating ion-exchange sorbents from various manufacturers, to select a desorbing solution and to determine the degree of desorption. The sorption of nickel and cobalt was carried out in a weakly acidic medium from a model solution containing impurities of other metals in static and dynamic modes. The limiting sorption capacity for the studied sorbents is 18-26 mg/g for nickel and 1-2 mg/g for cobalt in the static mode. The sorption capacity in the dynamic mode for nickel is equal to 25.5 g/L for Purolite S 930, 29.2 g/L for Lewatit TP 207, 1.4 g/L, and 1.8 g/L for cobalt, respectively. The best desorption parameters are achieved when using a 2 M sulfuric acid solution. The degree of desorption for sorbents Purolite S 930 and Lewatit TP 207 exceeds 90%. The use of the Lewatit TP 207 sorbent for the extraction of nickel from the leaching solution of nickel ore of the Gornostaevskoye deposit in 5 cycles made it possible to obtain a commercial desorbate with a nickel content of 18 g/L. The use of a part of the commercial desorbate obtained in the previous cycle, further strengthened to the initial concentration of sulfuric acid, for re-extracting nickel from the saturated sorbent during a cyclic process leads to a deterioration in desorption characteristics. It is recommended to remove the commercial desorbate from the process after several cycles of desorption and supply new solution of sulfuric acid for desorption to restore the sorption parameters.
从Gornostaevskoye矿床矿石中提取镍和钴吸附材料的选择
氧化镍矿占适合镍生产的工业矿石的大多数。由于镍含量低,使用传统火法冶金技术处理此类矿石在经济上是不可行的。处理氧化镍矿最具成本效益的方法之一是硫酸浸出技术,然后是吸附萃取。这项工作的目的是建立使用不同制造商的亚氨基二乙酸螯合离子交换吸附剂吸附萃取镍和钴的动力学和热力学参数,以选择解吸溶液并确定解吸程度。镍和钴的吸附是在弱酸性介质中从含有其他金属杂质的模型溶液中以静态和动态模式进行的。在静态模式下,所研究吸附剂对镍的极限吸附容量为18-26mg/g,对钴的极限吸附能力为1-2mg/g。在动态模式下,Purolite S 930对镍的吸附容量分别为25.5g/L、Lewatit TP 207对29.2g/L、钴对1.4g/L和1.8g/L。当使用2M硫酸溶液时,可以获得最佳的解吸参数。吸附剂Purolite S 930和Lewatit TP 207的解吸程度超过90%。使用Lewatit TP 207吸附剂在5个循环中从Gornostaevskoye矿床的镍矿浸出溶液中提取镍,使得可以获得镍含量为18g/L的商业脱附物。在循环过程中,使用在上一个循环中获得的部分商业脱附物,进一步强化到硫酸的初始浓度,用于从饱和吸附剂中重新提取镍,导致脱附特性恶化。建议在几个解吸循环后从工艺中去除商业解吸产物,并提供新的硫酸溶液进行解吸,以恢复吸附参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
17
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信